Non Clinical Jobs Jobs

Why This Role MattersPharmacovigilance plays a critical role in protecting patient safety by monitoring, detecting, and preventing adverse drug reactions. As a Pharmacovigilance Associate at Tata Consultancy Services, you will contribute directly to global drug safety operations, ensuring regulatory compliance and supporting pharmaceutical clients in maintaining high-quality safety standards. This role is essential in strengthening patient trust, maintaining regulatory integrity, and supporting life sciences innovation through structured safety monitoring and reporting.Job DescriptionTata Consultancy Services is hiring Pharmacovigilance Associates to support adverse event case processing, safety data management, and regulatory compliance activities. The selected candidate will be responsible for reviewing and processing Individual Case Safety Reports (ICSRs), performing drug safety data entry and validation, and ensuring accurate and timely submission of regulatory reports. The role requires hands-on experience with safety databases such as Argus or ARISg and strong knowledge of global pharmacovigilance regulations.Key Features of the Role:• Exposure to global pharmacovigilance operations• Opportunity to work with leading pharmaceutical clients• Hands-on experience with Argus Safety and ARISg databases• Involvement in signal detection and risk assessment support• Cross-functional collaboration within life sciences teams• Competitive salary structure aligned with industry standardsResponsibilities• Process and review adverse event case reports• Perform drug safety data entry and validation• Ensure compliance with global pharmacovigilance regulations• Work on safety databases such as Argus or ARISg• Conduct case follow-ups and resolve safety queries• Prepare and review case narratives• Maintain accuracy and completeness of safety data• Collaborate with cross-functional teams for safety reporting• Support signal detection and risk assessment activities• Participate in audits and regulatory inspections• Maintain documentation as per SOPs and guidelines• Ensure timely submission of regulatory reports• Identify discrepancies and resolve safety data issues• Assist in quality control and compliance checksRequired Qualifications• University Graduate (Life Sciences, Pharmacy, Biotechnology, Nursing, or related field preferred)• 2–4 years of experience in pharmacovigilance or drug safety• Experience in ICSR processing and case management• Hands-on knowledge of Argus Safety or ARISgEducational Requirements:• Bachelor’s degree in Pharmacy, Life Sciences, Biotechnology, or related discipline• Relevant certification in Pharmacovigilance preferredExperience and Skills:• Strong understanding of pharmacovigilance and drug safety processes• Expertise in ICSR case processing• Knowledge of global regulatory compliance requirements• Proficiency in Argus Safety or ARISg• Good understanding of medical terminology• Strong analytical and data review skills• Attention to detail and quality-focused mindset• Effective communication and documentation skills• Ability to work within defined timelines and SOP frameworksAge Eligibility:No specific age criteria mentioned. Candidates must meet educational and experience requirements.Salary Insights₹4,00,000 – ₹8,00,000 per annum (based on experience and expertise). Compensation may vary depending on candidate profile, project allocation, and skill level.Company OverviewTata Consultancy Services (TCS) is a global IT services, consulting, and business solutions organization delivering technology-driven solutions to leading enterprises worldwide. With a strong presence in life sciences and healthcare domains, TCS supports pharmaceutical and biotech organizations in pharmacovigilance, regulatory operations, clinical research, and digital transformation initiatives. TCS operates across multiple countries and is known for innovation, operational excellence, and client-centric solutions.FAQs1. Is experience in Argus mandatory?Experience in Argus or ARISg is strongly preferred.2. Is this a client-facing role?The role involves collaboration with internal and external stakeholders in safety reporting.3. Is remote work available?Location is specified as Mumbai / Pune; work model depends on project allocation.4. What growth opportunities are available?Career progression may include Senior PV Associate, Drug Safety Specialist, or Quality Reviewer roles.Application Tips• Highlight ICSR processing and case narrative experience clearly• Mention safety database expertise (Argus/ARISg) prominently• Showcase knowledge of global PV regulations• Quantify case volume handled per month if possible• Emphasize audit experience and compliance adherence• Tailor your CV specifically for pharmacovigilance keywords

Why This Role MattersThe Project Manager – Pharmacovigilance plays a mission-critical role in ensuring the highest standards of quality, compliance, and patient safety within Inizio Ignite’s advisory and consulting operations. In the evolving life sciences landscape, pharmacovigilance compliance is not just a regulatory requirement but a strategic enabler of trust, scientific integrity, and patient impact. This role supports Putnam Associates and broader advisory teams by strengthening adverse event reporting, audit readiness, and compliance governance frameworks. By ensuring adherence to global pharmacovigilance standards such as GVP, FDA, and EMA guidelines, the role directly contributes to safeguarding patients, protecting client reputation, and maintaining regulatory excellence. In a fast-paced consulting environment, this position ensures that operational efficiency and regulatory precision coexist seamlessly, transforming compliance from a reactive function into a proactive strategic advantage.Job DescriptionThe Project Manager – Pharmacovigilance (Quality, Risk & Compliance) will oversee and support the execution of pharmacovigilance compliance and reporting processes within Inizio Ignite’s Operational Efficiency and Effectiveness function. The role involves collaboration with consulting teams, clients, and cross-functional stakeholders to ensure adverse event processing, audit management, training compliance, and documentation standards meet global regulatory expectations. The individual will act as a compliance partner to consulting case teams, ensuring pharmacovigilance agreements, safety management plans, and quality processes are executed accurately and efficiently. The role demands strong project management capabilities, regulatory understanding, and a proactive mindset to identify, mitigate, and escalate compliance risks.Key Features of the Role:• Hybrid working model based in Gurugram• Strategic exposure to global life sciences clients• Direct involvement in pharmacovigilance compliance governance• Cross-functional collaboration with consulting, risk, and regulatory teams• Audit readiness and CAPA leadership responsibilities• Opportunity to drive process improvement and operational excellenceResponsibilities• Support case management activities to ensure timely and accurate AE processing• Assist in pre-audit preparation, audit coordination, and post-audit CAPA management• Lead internal audit preparedness initiatives for client engagements• Monitor implementation of pharmacovigilance agreements and safety management plans• Maintain and manage CAPA trackers, ensuring timely closure of corrective actions• Conduct compliance training for consulting teams and track completion status• Review and support submission of AE/SAE reconciliations and project close-out documentation• Maintain project milestone repositories and compliance documentation archives• Coordinate compliance requirements across multiple client engagements• Provide content guidance for safety documentation and regulatory reporting• Support vendor training on client PV compliance standards• Address technical and operational issues related to PV client platforms• Assist in development and revision of SOPs, compliance policies, and best practices• Identify compliance risks proactively and escalate critical concerns appropriatelyRequired Qualifications• Demonstrated experience in pharmacovigilance case management or compliance• Familiarity with global PV regulations including GVP, FDA, and EMA requirements• Strong understanding of audit management and CAPA processes• Experience working in consulting or client-facing environments preferred• Proficiency in Microsoft Office tools including Excel, PowerPoint, and Word• Smartsheet familiarity preferredEducational Requirements:• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or Business• Advanced degree preferred but not mandatoryExperience and Skills:• Minimum 2 years of relevant experience in pharmacovigilance or regulatory compliance• Strong documentation and process improvement orientation• Excellent project management and organizational skills• High attention to detail and analytical thinking ability• Ability to interpret regulatory guidelines and implement compliance processes• Strong communication and stakeholder engagement skills• Ability to work independently in a fast-paced, growth-oriented environment• Agile mindset with strong business acumenAge Eligibility:No specific age criteria are mentioned. Candidates must meet educational and professional qualification requirements.Salary InsightsCompensation is competitive and aligned with industry standards for pharmacovigilance project management roles in India. Salary may vary based on experience, expertise in regulatory compliance, and consulting exposure. Additional benefits may include performance incentives, hybrid work flexibility, and professional development opportunities.Company OverviewInizio Ignite is part of the global Inizio group, a leading partner to health and life sciences organizations. With over 10,500 experts across more than 50 countries, Inizio supports companies across the product lifecycle from early development to commercialization and beyond. Inizio Ignite combines strategy, innovation, research partnership, and consulting expertise to drive transformation in healthcare. Through its Putnam strategy consulting arm, the organization bridges science and strategy, enabling confident decision-making for pharmaceutical, biotech, and medical device clients. Guided by purpose, precision, and passion, Inizio Ignite is committed to delivering measurable impact while fostering diversity, inclusion, and innovation within its global workforce.FAQIs this role client-facing? Yes, the role involves collaboration with client teams and consulting case teams to ensure PV compliance alignment.Is prior pharmacovigilance experience mandatory? Yes, demonstrated experience in PV case management or compliance is required.Does the role require travel? Travel requirements may vary depending on audit and client engagement needs.Is this a leadership role? This role provides leadership in audit preparedness, CAPA management, and compliance governance within consulting engagements.Is remote work allowed? The position follows a hybrid work model in GurugramApplication Tips• Highlight pharmacovigilance case management and compliance experience clearly in your CV• Demonstrate familiarity with GVP, FDA, and EMA regulatory frameworks• Showcase audit experience, CAPA management, and SOP development exposure• Emphasize cross-functional collaboration and consulting exposure• Quantify achievements such as audit readiness improvements or compliance efficiency gains• Tailor your resume to highlight regulatory precision, project management capabilities, and analytical strengths

Why This Role MattersThe Pharmacist Manager plays a pivotal leadership role in ensuring the safe, compliant, and efficient operation of a community pharmacy. Beyond dispensing medicines, this role shapes team culture, strengthens community relationships, and drives professional service delivery.This position offers the opportunity to lead an established pharmacy with a loyal customer base, allowing you to focus on patient-centred care, operational excellence, and long-term business growth.Job DescriptionA Full-Time Pharmacist Manager is required to lead a well-established Good Price Pharmacy in Morphett Vale. The successful candidate will oversee daily pharmacy operations, mentor a dedicated team, and ensure compliance with professional and legislative requirements.This role offers strong operational support, leadership autonomy, and a genuine work–life balance with no weekend work. It is ideal for an experienced pharmacist ready to step into or continue in a leadership position within a progressive and growing pharmacy group.Key Features of the Role• Full-time leadership position• No weekend work – weekday schedule• Established customer base and strong community presence• Supportive and experienced team• Leadership autonomy with structured operational support• Ongoing professional development opportunitiesResponsibilities• Lead and mentor pharmacists, technicians, and support staff• Oversee daily dispensary operations and workflow management• Ensure accurate and compliant dispensing of prescription medicines• Deliver exceptional customer and patient-centred care• Implement and oversee professional pharmacy services• Maintain compliance with AHPRA standards and relevant pharmacy legislation• Manage stock control, ordering, and inventory systems• Monitor KPIs and drive continuous operational improvement• Foster strong relationships within the local community• Promote a positive, collaborative, and team-oriented culture• Ensure adherence to professional and ethical standardsEducational and Registration Requirements• Bachelor of Pharmacy – Mandatory• Current general registration with the Australian Health Practitioner Regulation Agency (AHPRA) – Mandatory• Full Australian working rightsExperience and SkillsExperience:• Minimum 3 years’ experience as an AHPRA-registered pharmacist• Experience managing a busy dispensary• Prior leadership or supervisory experience preferredTechnical Skills:• Strong understanding of dispensing software systems• Knowledge of PBS processes and regulatory compliance• Experience implementing professional pharmacy servicesLeadership and Behavioral Skills:• Excellent communication and interpersonal abilities• Strong organisational and time-management skills• Ability to lead, motivate, and mentor a team• High level of teamwork and collaboration• Initiative and decision-making capability• Ability to create a positive, performance-driven environmentWork Schedule• Full-time position• No weekend work• Stable weekday operationsSalary and Benefits• Competitive remuneration package• Stable, full-time employment• Ongoing training and professional development• Strong local operational support• Positive and collaborative workplace culture• Opportunity to grow within a progressive pharmacy groupCompany OverviewGood Price Pharmacy Warehouse is one of Australia’s leading retailers in health, beauty, and medicinal products, offering trusted brands at competitive prices. Operating under Scaffidi Pharmacy Services, the organisation provides strong operational support, professional development opportunities, and a collaborative network across its pharmacy group.FAQsIs weekend work required?No. This is a weekday-only position, offering strong work–life balance.Is prior management experience mandatory?While formal title experience is preferred, candidates with strong leadership exposure in busy dispensaries will be considered.Are professional services part of the role?Yes. The Pharmacist Manager is expected to oversee and implement professional pharmacy services.Is visa sponsorship available?Applicants must currently reside in Australia with full working rights.What kind of team support is provided?You will work with an established, skilled team and receive structured operational support from the group.Application Tips• Highlight leadership and team management experience• Clearly mention AHPRA registration details• Showcase experience managing high-volume dispensary operations• Provide examples of professional services delivered• Emphasise community engagement and patient care achievements

🚀 We’re Hiring: Program Manager – Medical Education(For MBBS / MD / BDS / MDS / PharmD Professionals)A High-Impact Non-Clinical Leadership Career📍 Location: Dehradun / Work From Home🕒 Experience: 0–5 Years💼 Full-Time | Healthcare EdTech | Management Track👨‍⚕️ For Doctors Ready to Expand Their ImpactAre you a qualified MBBS / MD / BDS / MDS / PharmD professional who:✔ Wants to move beyond repetitive clinical routines?✔ Believes your expertise deserves larger influence?✔ Is curious about leadership, strategy, and education?✔ Wants to build authority beyond hospital walls?This is your opportunity to transition into a high-growth, non-clinical leadership role.🌍 About Academically GlobalAcademically Global is a rapidly scaling Healthcare EdTech platform helping doctors and healthcare professionals build global, high-income careers.Founded and led by Dr. Akram Ahmad, an internationally recognized healthcare career mentor with 1M+ followers, we specialize in:✔ Global licensing exam preparation (Australia & beyond)✔ Industry upskilling programs✔ Study-abroad and non-clinical pathways✔ Career transition guidance for healthcare professionalsWe are now expanding our Medical & Non-Clinical Education Vertical and we are looking for a doctor who can help build and lead it.🔑 Your Role & Impact📌 Strategic LeadershipIdentify high-demand medical & healthcare programsDesign scalable, market-driven education modelsDefine KPIs, budgets, and growth roadmapsContinuously optimize programs for scale and sustainability📚 Academic ExcellenceCollaborate with Academic Heads & Subject Matter ExpertsEnsure globally aligned, practical, and industry-relevant curriculumMaintain academic integrity and outcome-driven learning🎤 Thought Leadership & VisibilityConduct webinars, workshops & live sessionsRepresent Academically on digital platformsMentor doctors exploring global and non-clinical careers🤝 Cross-Functional OwnershipWork with Marketing, Sales & Tech teamsDrive launches and go-to-market strategiesTrack learner outcomes, engagement, and program impact✅ Ideal Candidate ProfileMBBS (Mandatory) | MD preferredBDS / MDS / PharmD also eligibleMBA / MPH (added advantage)0–5 years experience (Clinical / Academic / Program roles)Strong business mindset & startup adaptabilityComfortable on camera & public platformsPassionate about mentoring and education innovation🌟 Why This Role Stands OutThis is not a routine administrative job.This is a career transition opportunity where you:✔ Move into leadership without leaving healthcare✔ Influence thousands of professionals globally✔ Build a new vertical from ground up✔ Work directly with a fast-scaling founder-led brand✔ Develop business, strategy, and brand authority

Why This Role MattersPatient safety is the foundation of clinical research and pharmaceutical development. Pharmacovigilance ensures that adverse events are properly monitored, assessed, and reported in compliance with global regulatory standards. Effective safety oversight not only protects patients participating in clinical trials but also safeguards public health after products reach the market.The Supervisor – Pharmacovigilance role at ICON plc is central to maintaining high standards of drug safety reporting and regulatory compliance. This position directly influences the accuracy, timeliness, and integrity of adverse event reporting while leading a team responsible for critical safety operations.For professionals with strong pharmacovigilance experience and leadership capabilities, this role offers the opportunity to contribute to global clinical development programs within a world-leading healthcare intelligence and clinical research organization.Job DescriptionICON plc is seeking a Supervisor – Pharmacovigilance to join its dynamic and diverse team. The selected candidate will oversee day-to-day pharmacovigilance operations related to clinical trials and marketed products. The role involves supervising safety reporting processes, ensuring regulatory compliance, managing submission workflows, and guiding the pharmacovigilance team to maintain best-in-class reporting standards.The Supervisor will collaborate with cross-functional departments including clinical operations, regulatory affairs, and quality teams to optimize safety reporting systems and maintain compliance with global pharmacovigilance regulations. This position requires strong technical knowledge, leadership skills, and the ability to manage multiple safety workflows simultaneously.Key Features of the RoleLeadership opportunity within global pharmacovigilance operations.Exposure to clinical trial and post-marketing safety reporting.Direct interaction with regulatory authorities and global compliance frameworks.Collaboration with cross-functional global teams.Career progression within a leading clinical research organization.Responsibilities RequiredSupervise day-to-day pharmacovigilance safety reporting operations, ensuring timely and accurate submission of adverse event reports to regulatory authorities.Oversee safety case processing, medical review coordination, and submission tracking in accordance with global regulatory timelines.Ensure compliance with international pharmacovigilance regulations, guidelines, and internal standard operating procedures (SOPs).Manage safety submissions workflow and ensure proper documentation, quality checks, and audit readiness.Collaborate with clinical operations, regulatory affairs, and quality assurance teams to streamline safety reporting processes.Provide leadership, mentoring, and training to pharmacovigilance team members to ensure adherence to best practices.Monitor performance metrics and implement process improvements to enhance reporting efficiency and compliance.Support regulatory inspections and audits by preparing required documentation and addressing safety-related queries.Ensure accurate maintenance of safety databases and tracking systems.Identify potential compliance risks and implement corrective and preventive actions (CAPA) where required.Maintain high standards of data accuracy, confidentiality, and regulatory integrity across all pharmacovigilance activities.QualificationsThe ideal candidate will possess a strong academic background in life sciences or pharmacy, combined with practical pharmacovigilance and leadership experience.Educational Requirements:Bachelor’s degree in Life Sciences, Pharmacy, or a related field.Experience and Skills:Solid experience in pharmacovigilance or drug safety, particularly in clinical trials and/or post-marketing surveillance.Strong knowledge of global pharmacovigilance regulations and reporting guidelines (e.g., ICH, FDA, EMA frameworks).Experience supervising or mentoring pharmacovigilance team members.Strong understanding of safety database systems and submission workflows.Excellent communication and organizational skills.Ability to manage multiple priorities and ensure compliance with strict regulatory timelines.High attention to detail and commitment to data accuracy.Ability to work effectively in a cross-functional and global team environment.Salary InsightsCompensation will be competitive and aligned with global CRO industry standards for supervisory-level pharmacovigilance professionals. The overall package may include performance-based incentives and country-specific benefits aligned with experience and role responsibility.Additional benefits may include:Competitive salary structureHealth insurance options for employees and familiesRetirement planning benefitsLife assurance coverageGlobal Employee Assistance Programme (LifeWorks)Flexible, country-specific optional benefits such as childcare vouchers, gym memberships, and travel subsidiesGenerous annual leave entitlementsCompany OverviewICON plc is a world-leading healthcare intelligence and clinical research organization dedicated to advancing clinical development and improving patient outcomes. The company operates globally, supporting pharmaceutical, biotechnology, and medical device clients in delivering high-quality clinical research solutions.ICON fosters a culture of inclusion, innovation, and excellence, providing professionals with opportunities to grow within a diverse and performance-driven environment. The organization is committed to maintaining a workplace free from discrimination and promoting equal opportunity for all employees.FAQsIs supervisory experience mandatory for this role?Yes, prior experience in leading or mentoring pharmacovigilance teams is highly preferred.Does this role focus only on clinical trials?The role covers both clinical trial safety reporting and post-marketing surveillance activities.What regulatory knowledge is required?Strong knowledge of global pharmacovigilance regulations such as ICH guidelines and regulatory authority requirements (e.g., FDA, EMA).Are cross-functional collaborations involved?Yes, the role requires close coordination with clinical operations, regulatory affairs, and quality teams.What is the primary objective of the role?To ensure accurate, timely, and compliant safety reporting while leading pharmacovigilance operations effectively.Application TipsHighlight your pharmacovigilance experience, especially supervisory or leadership responsibilities.Mention regulatory frameworks and safety databases you have worked with.Provide examples of managing submission timelines and regulatory compliance.Demonstrate experience handling audits or inspections related to safety reporting.Be prepared to discuss real-world pharmacovigilance workflow management scenarios during the interview.

Why This Role MattersThe Medical Scientific Liaison (MSL) role at Baxter International Inc. is a strategic, field-based position that directly influences scientific engagement, clinical understanding, and healthcare advancement. As a global healthcare company founded on the mission to “Save and Sustain Lives,” Baxter focuses on improving outcomes in critical care, surgery, anesthesia, renal care, and other life-saving therapeutic areas. The MSL serves as the scientific bridge between Baxter and healthcare professionals (HCPs), ensuring accurate, ethical, and evidence-based communication of clinical data.This role matters because it strengthens Baxter’s scientific credibility within the medical community. By engaging in high-quality scientific exchange, supporting evidence generation, and gathering real-world insights, the MSL contributes to better-informed clinical decisions and enhanced patient outcomes. In a rapidly evolving healthcare landscape, this position ensures that innovation translates effectively into clinical practice.Job DescriptionThe Medical Scientific Liaison is a field-based medical expert responsible for engaging healthcare professionals through scientific discussions, clinical data interpretation, and insight gathering. The role supports medical strategy execution, evidence dissemination, and cross-functional collaboration.The MSL will translate clinical data into practical knowledge for healthcare professionals while supporting internal commercial and medical teams with strategic insights. The candidate must be proactive, scientifically driven, and capable of independently managing stakeholder relationships across hospitals, academic institutions, and healthcare networks.Key Features of the Role• Position: Medical Scientific Liaison• Organization: Baxter International Inc.• Location: Gurgaon, Haryana, India• Employment Type: Full-time• Field-based role with domestic and international travel• Engagement with Key Opinion Leaders (KOLs)• Cross-functional collaboration with medical and commercial teamsResponsibilities• Lead and execute local and regional medical strategies aligned with business objectives• Engage healthcare professionals through scientific exchange and education• Present and discuss clinical evidence supporting Baxter therapeutics• Collect and analyze field insights to inform internal strategy• Support real-world data generation and investigator-initiated research• Organize and facilitate advisory boards and scientific meetings• Develop and deliver internal training for commercial and cross-functional teams• Review promotional materials and ensure compliance with medical regulations• Participate in cross-functional initiatives as a medical reviewer• Build and maintain long-term professional relationships with KOLs• Monitor therapeutic landscape developments and emerging evidence• Ensure all activities meet ethical and regulatory compliance standardsRequired QualificationsTo perform successfully in this role, the candidate must demonstrate strong scientific expertise, communication capability, and strategic thinking. The individual should possess the ability to operate independently in a dynamic, fast-paced field environment while maintaining high professional integrity.Educational Requirements• MBBS degree or• Master’s or PhD in Life Sciences or• Pharmacy degree or country equivalentAll qualifications must be from recognized institutions and aligned with industry standards.Experience and Skills• Minimum 2 years of experience in Medical Affairs, Clinical Development, or Market Access within a pharmaceutical or medical device company• Experience in therapeutic areas such as anesthesia, surgical, or ICU environments is preferred• Strong understanding of clinical research methodology and evidence interpretation• Excellent scientific communication skills, both written and verbal• Professional fluency in English• Strong interpersonal skills to engage diverse stakeholders• High business acumen and strategic thinking capability• Ability to manage multiple priorities and cross-functional requests• Resilience and adaptability in field-based roles• Organizational skills and sound judgment in decision-making• Commitment to continuous professional developmentAge EligibilityAge criteria are not specified. Candidates must meet qualification and professional experience requirements as outlined in the role.Salary InsightsSalary details are not publicly disclosed. Compensation will be aligned with industry standards for Medical Scientific Liaison roles within multinational pharmaceutical and medical device companies. Baxter offers competitive remuneration packages reflecting experience, expertise, and strategic impact.Company OverviewBaxter International Inc. is a global healthcare leader established in 1931. Headquartered in the United States, Baxter focuses on advancing patient care through innovative medical products and therapies. The company operates across multiple therapeutic areas including critical care, renal care, surgical solutions, and hospital products. Baxter’s mission, “Save and Sustain Lives,” guides its operations worldwide.The organization fosters a culture of courage, collaboration, accountability, and continuous improvement. Baxter is committed to diversity, equal employment opportunity, and providing reasonable accommodations for individuals with disabilities. The company maintains strict ethical standards and actively protects applicants from recruitment fraud.FAQsIs this a field-based role? Yes, it requires engagement with healthcare professionals and travel as needed.What educational background is required? MBBS, Pharmacy, or Master/PhD in Life Sciences.Is prior industry experience mandatory? Yes, at least 2 years in a pharmaceutical or medical device company.What therapeutic experience is preferred? Anesthesia, surgical, or ICU environments.Does the role involve compliance responsibilities? Yes, including medical review of materials and ethical oversight.Application Tips• Highlight Medical Affairs or clinical development experience• Emphasize KOL engagement and scientific communication expertise• Demonstrate experience in evidence interpretation and real-world data• Showcase leadership in advisory boards or cross-functional initiatives• Prepare examples of field-based scientific engagement• Ensure your CV reflects measurable impact in previous roles• Be prepared to discuss compliance knowledge and stakeholder management skills

Why This Role MattersIn modern healthcare systems, timely access to medication depends not only on clinical accuracy but also on efficient insurance coordination and regulatory compliance. Delays in insurance verification, prior authorization approvals, or claim processing can directly impact patient treatment outcomes and satisfaction.The Pharmacy Insurance & Prior Authorization Executive role at Zulekha Hospital LLC plays a crucial role in ensuring seamless medication access while minimizing financial burden on patients. By verifying eligibility, managing prior authorizations, resolving claim denials, and maintaining PBM compliance, this position strengthens both patient care delivery and revenue cycle efficiency.This role is ideal for professionals with pharmacy or healthcare administration backgrounds who have experience handling insurance processes within hospital or pharmacy environments.Job DescriptionZulekha Hospitals, UAE (JCI Accredited and Winner of the Dubai Quality Award), is one of the largest healthcare providers in the region. With two multi-disciplinary hospitals in Sharjah and Dubai, four medical centers, and three pharmacies, the organization delivers high-quality healthcare services supported by advanced diagnostic facilities and super specialty units including Cardiac Care, ICU, and NICU.The hospital is currently seeking a skilled Pharmacy Insurance & Prior Authorization Executive to manage insurance verification, prior authorization processing, PBM compliance, and billing resolution processes within its pharmacy operations. The selected candidate will ensure accurate insurance coordination while maintaining regulatory compliance and high service standards.Key Features of the RoleDirect involvement in patient access and insurance coordination processes.Exposure to PBM policies and healthcare insurance regulations.Opportunity to work in a JCI-accredited healthcare environment.Engagement with cross-functional teams including pharmacists, physicians, and billing departments.Contribution to reducing claim denials and improving revenue cycle performance.Responsibilities RequiredVerify patient insurance eligibility and benefits to ensure seamless medication access and minimize out-of-pocket costs.Process prior authorization requests accurately and efficiently, coordinating with healthcare providers to collect required clinical documentation.Communicate with insurance companies and Pharmacy Benefit Managers (PBMs) to facilitate approvals and resolve coverage issues.Resolve billing discrepancies and insurance denials by conducting root cause investigations and following up with payers for timely resolution.Maintain up-to-date knowledge of PBM policies, insurance guidelines, and regulatory requirements to ensure compliance and optimal service delivery.Submit and track claims while ensuring proper documentation and adherence to internal billing procedures.Support patients by explaining insurance coverage details and authorization requirements clearly and professionally.Collaborate with pharmacists, physicians, and administrative teams to streamline medication approval workflows.Maintain accurate records of prior authorizations, claim submissions, denials, and resolution outcomes.Ensure compliance with healthcare data privacy standards and internal hospital policies.Contribute to continuous improvement initiatives aimed at reducing turnaround time for approvals and minimizing claim rejections.QualificationsThe ideal candidate should have strong knowledge of pharmacy insurance processes, billing systems, and regulatory frameworks within healthcare environments.Educational Requirements:Bachelor’s degree in Pharmacy, Health Administration, or a related healthcare field (preferred).Relevant certifications such as Certified Pharmacy Technician (CPhT) or Medicare/Medicaid certification are advantageous.Experience and Skills:Minimum 2 years of experience in a pharmacy or hospital setting with focus on insurance coordination or billing processes.Experience working with various insurance systems and understanding pharmacy benefit structures.Knowledge of prior authorization processes and PBM policies.Strong analytical skills to investigate billing discrepancies and claim denials.Excellent communication skills for interacting with patients, providers, and insurance representatives.Familiarity with healthcare compliance standards and data privacy regulations.Ability to manage multiple claims and authorization requests efficiently.Attention to detail and strong documentation practices.Salary InsightsCompensation will be competitive and aligned with UAE healthcare industry standards for professionals with insurance coordination experience. Salary will depend on experience level, certifications, and operational expertise.Benefits may include:Competitive salary packageProfessional development opportunitiesExposure to accredited healthcare systemsStructured career growth within hospital operationsCompany OverviewZulekha Hospital LLC is a leading healthcare provider in the UAE, operating two multi-disciplinary hospitals in Sharjah and Dubai, along with multiple medical centers and pharmacies. The organization is JCI accredited and a recipient of the Dubai Quality Award, reflecting its commitment to excellence in healthcare delivery.With advanced super specialty units including Cardiac Care, ICU, and NICU, and comprehensive diagnostic facilities, Zulekha Hospitals is dedicated to delivering patient-centered care supported by strong administrative and compliance systems.FAQsIs prior authorization experience mandatory?Yes, candidates must have hands-on experience in insurance verification and prior authorization processes.Are pharmacy qualifications required?A Bachelor’s degree in Pharmacy or Health Administration is preferred, though related healthcare experience is also considered.What systems should candidates be familiar with?Insurance billing systems, PBM processes, and healthcare claim management platforms.Is certification required?Certifications like CPhT or Medicare/Medicaid credentials are advantageous but not mandatory.What is the primary focus of the role?Ensuring seamless medication access by managing insurance verification, prior authorization approvals, and billing compliance.Application TipsHighlight your experience with insurance systems and prior authorization handling.Mention PBM knowledge and any certifications obtained.Provide examples of claim denial resolutions or billing discrepancy investigations handled.Demonstrate strong communication skills and patient interaction experience.Be prepared to discuss real-life scenarios related to insurance coordination and compliance management.

Why This Role MattersIn pharmaceutical manufacturing, especially within Oral Solid Dosage (OSD) facilities, analytical quality oversight is critical to ensuring patient safety, product consistency, and regulatory compliance. Every batch released to the market must meet stringent quality standards supported by scientifically verified analytical data.The Analytical QA Executive role at Ontop Pharmaceuticals Private Limited plays a pivotal role in strengthening data integrity, reviewing analytical outputs, and ensuring that laboratory operations comply with GLP and cGMP standards. This position directly impacts batch release decisions, regulatory inspection readiness, and overall quality system robustness.For professionals with hands-on analytical experience in OSD plants, this opportunity offers strong exposure to quality systems, compliance management, and regulatory-driven manufacturing operations in WHO-GMP and Schedule M compliant facilities.Job DescriptionOntop Pharmaceuticals Private Limited, a WHO-GMP and Schedule M compliant pharmaceutical manufacturer with facilities in Bengaluru and Hyderabad, is expanding its Quality Assurance team. The organization specializes in high-quality oral solid dosage formulations and is seeking experienced professionals for the role of Analytical QA Executive.The selected candidate will be responsible for reviewing analytical data, handling investigations related to OOS and OOT results, ensuring GLP and cGMP compliance, and supporting regulatory adherence within the OSD manufacturing setup. The role demands technical expertise in chromatographic and spectroscopic data review, strong documentation practices, and the ability to maintain high standards of data integrity.This position is ideal for candidates with 2–3 years of experience in Analytical QA or QC within OSD plants who are looking to advance their careers in quality assurance and compliance-driven environments.Key Features of the RoleOpportunity to work in WHO-GMP and Schedule M compliant manufacturing facilities.Direct exposure to analytical review processes in OSD manufacturing.Hands-on involvement in OOS/OOT investigations and CAPA management.Strong focus on regulatory compliance and data integrity practices.Career growth opportunities in quality assurance within a structured pharmaceutical setup.Positions available in Bengaluru and Hyderabad manufacturing sites.Responsibilities RequiredPerform analytical QA oversight activities in an OSD manufacturing plant to ensure compliance with internal quality standards and regulatory requirements.Review analytical data generated from techniques such as HPLC, GC, UV spectrophotometry, and dissolution testing for accuracy, completeness, and compliance.Verify raw data, chromatograms, system suitability parameters, and calculations to ensure correctness and adherence to validated methods.Handle Out of Specification (OOS) and Out of Trend (OOT) investigations in coordination with QC and production teams, ensuring root cause analysis and timely closure.Initiate and track Corrective and Preventive Actions (CAPA) to address deviations and improve system robustness.Ensure compliance with Good Laboratory Practices (GLP) and current Good Manufacturing Practices (cGMP) across analytical operations.Maintain strict data integrity standards in accordance with regulatory expectations, including audit trail review and documentation control.Participate in internal audits and support regulatory inspections by providing required documentation and analytical justifications.Review analytical method validation, verification, and stability study reports to ensure compliance with regulatory and internal guidelines.Collaborate with cross-functional teams including QC, production, and QA to maintain seamless quality operations.Ensure adherence to SOPs, quality management systems (QMS), and documentation control procedures.Support continuous improvement initiatives to enhance laboratory compliance and efficiency.QualificationsCandidates must demonstrate strong analytical knowledge, regulatory awareness, and hands-on OSD plant experience.Educational Requirements:Bachelor's degree in Pharamcy (B.Pharm), Matser's degree in Pharmacy (M.Pharm), or related life sciences qualification from a recognized institution.Experience and Skills:2–3 years of experience in Analytical QA or QC, preferably within an OSD manufacturing plant.Proficiency in reviewing analytical data from HPLC, GC, UV, and dissolution studies.Strong understanding of OOS, OOT handling, and CAPA implementation.Knowledge of GLP, cGMP, Schedule M, and WHO-GMP compliance standards.Familiarity with data integrity principles and regulatory documentation practices.Strong attention to detail and analytical problem-solving skills.Good documentation, communication, and cross-functional coordination abilities.Ability to manage multiple analytical reviews and investigations within defined timelines.Preference may be given to local candidates from Bengaluru or Hyderabad and immediate joiners.Salary InsightsWhile exact compensation is not disclosed, typical salary ranges for Analytical QA Executives with 2–3 years of experience in Bengaluru or Hyderabad fall between ₹4–7 lakhs per annum, depending on expertise, technical proficiency, and negotiation.Compensation may include:Competitive industry-aligned salaryOpportunities for performance-based growthExposure to regulated manufacturing environmentsProfessional development within QA systemsCompany OverviewOntop Pharmaceuticals Private Limited is a well-established pharmaceutical manufacturer operating WHO-GMP and Schedule M compliant facilities in Bengaluru and Hyderabad. The company specializes in producing high-quality oral solid dosage (OSD) formulations with a strong emphasis on regulatory compliance, quality excellence, and data integrity.With a focus on robust quality systems and manufacturing standards, Ontop Pharmaceuticals provides professionals with opportunities to grow in compliance-driven environments while contributing to the production of safe and effective pharmaceutical products.FAQsWhat experience is required for this role?Candidates must have 2–3 years of experience in Analytical QA or QC, preferably in an OSD plant.Is OSD experience mandatory?Experience in an OSD manufacturing setup is strongly preferred.What analytical techniques should candidates be familiar with?HPLC, GC, UV spectrophotometry, and dissolution testing data review experience is required.Are local candidates preferred?Yes, candidates based in Bengaluru or Hyderabad are preferred, along with immediate joiners.What compliance knowledge is essential?Knowledge of GLP, cGMP, Schedule M, WHO-GMP, OOS/OOT handling, CAPA, and data integrity is essential.Application TipsClearly highlight your OSD plant experience in your resume.Mention specific analytical instruments handled and data review exposure.Include examples of OOS investigations and CAPA involvement.Demonstrate understanding of data integrity and regulatory compliance principles.Prepare to discuss real-time analytical review scenarios and compliance challenges during the interview.

Why This Role MattersThe Injury and Claims Advisor role at Metro Trains Melbourne is critical in supporting the health, safety, and wellbeing of employees across one of Australia’s largest rail networks. This position ensures effective management of workplace injuries and workers’ compensation claims while promoting sustainable return-to-work outcomes that protect both staff and organisational interests. By providing expert guidance and coordinating injury management plans, this role reduces the long-term impact of injuries and enhances workplace rehabilitation practices, contributing directly to a safer work environment and positive employee experience.Job DescriptionThe Injury and Claims Advisor will manage all aspects of workplace injury and compensation claims from initial lodgement to resolution. This includes providing expert advice on injury and claims processes, developing return-to-work plans, ensuring compliance with relevant legislation, collaborating with stakeholders, and delivering actionable insights to improve claims outcomes and processes across the organisation.Key Features of the Role• Position: Injury and Claims Advisor• Company: Metro Trains Melbourne• Location: Docklands, Victoria, Australia• Employment Type: Full-Time, Permanent• Work Environment: Corporate / Health & Wellbeing Division• Reports To: Head of Health & Wellbeing• Focus: Injury management, workers’ compensation, return-to-work coordination• Benefits: Inclusive workplace, flexible work options, complimentary travel pass, corporate discountsResponsibilities• Manage workers’ compensation claims from notification through to closure• Develop return-to-work plans in collaboration with injured employees, managers, and healthcare providers• Provide expert advice on injury management, claims processes, and return-to-work policies• Act as the primary contact for external stakeholders including WorkSafe agents, healthcare providers, and legal teams• Track and analyse claim trends, monitor costs, and recommend process improvements• Maintain accurate and comprehensive documentation of all claims activities• Support compliance audits and reporting related to injury and claims management• Build strong working relationships with internal stakeholders to promote engagement and best practicesRequired QualificationCandidates must have the necessary academic and professional background to manage injury and claims processes within a complex organisational environment.Educational Requirement•Qualification in Occupational Rehabilitation, Personal Injury Management, Allied Health, or Mental Health is advantageous• Strong understanding of workers’ compensation legislation and injury management frameworks relevant to Victoria, AustraliaImportant Remarks• Experience in a similar injury, claims, or rehabilitation role is highly preferred• The role requires impartial judgement, strong stakeholder engagement abilities, and the capacity to manage sensitive workplace injury cases• Applicants should be prepared to work within a fast-paced and compliance-focused corporate environmentExperience and SkillsExperience Required• Minimum of 2 years’ experience in workers’ compensation, injury management, or claims management roles• Practical experience handling complex injury cases and developing return-to-work programsKey Skills Expected• Strong knowledge of injury and claims legislation and compliance standards• Excellent communication and interpersonal skills• Ability to build relationships and influence internal and external stakeholders• High attention to detail and prioritisation skills• Ability to work independently and manage multiple cases effectively• Problem-solving skills and a customer-focused approachAge Eligibility• Not specified by the employerSalary Insights• Competitive remuneration (specific salary details are not publicly disclosed)• Employee benefits such as a free transport pass and flexible working options are part of the total packageCompany OverviewMetro Trains Melbourne operates and maintains the metropolitan rail network in Melbourne, Australia, prioritising safety, customer service, and operational excellence. The company employs thousands of diverse professionals across technical, operational, and corporate roles, fostering a supportive and inclusive workplace culture that values development, innovation, and community engagement.FAQsIs injury and claims experience mandatory?Yes — experience in workers’ compensation and injury management is important for success in this role.What qualifications are valuable?Qualifications in occupational rehabilitation, injury management, or allied health are advantageous.Is this role full-time?Yes — this is a full-time, permanent position.Does the role involve external stakeholder management?Yes — including working with WorkSafe agents and healthcare providers.Is employee wellbeing part of the focus?Yes — promoting health, wellbeing, and sustainable return-to-work outcomes is central to the role.Application Tips• Highlight your experience in workers’ compensation and injury management in your CV• Mention specific legislation or frameworks you are familiar with (e.g., Workplace Injury Rehabilitation and Compensation Act)• Demonstrate examples of return-to-work plans you have developed• Emphasise your communication and stakeholder engagement skills• Prepare to discuss how you manage sensitive and complex cases in interviews

Why This Role MattersThe Physio Manager-MPT role at Portea Medical is an important position that ensures efficient patient care delivery and smooth operational functioning of physiotherapy services. This role supports clinicians by coordinating patient scheduling, tracking follow-ups, and managing daily clinic workflow — directly influencing treatment experiences and patient satisfaction. Applicants with a background in physiotherapy and healthcare operations can bring structure, organisation, and enhanced service quality to a busy clinical setting.Job DescriptionThe Physio Manager-MPT will oversee patient coordination, appointment scheduling, follow-ups, documentation, and basic operational activities to ensure a seamless physiotherapy treatment experience. This role involves close collaboration with physiotherapists and the operations team, and requires strong communication and organisation skills.Key Features of the Role• Position: Physio Manager-MPT• Company: Portea Medical• Location: Domlur, Bengaluru, Karnataka, India• Employment Type: Full-Time• Work Setting: In-person clinical operations• Benefits: Health insurance, Provident Fund• Focus: Patient care coordination & ops support• Salary: Depends on last drawn / experience (not fixed)Responsibilities• Manage patient interaction and coordination for physiotherapy appointments• Schedule and update patient appointments• Coordinate therapist workload planning• Conduct patient follow-ups and treatment tracking• Handle patient queries, feedback, and consent documentation• Maintain basic reporting and documentation processes• Work closely with physiotherapists to enable seamless care deliveryRequired QualificationCandidates must have the necessary physiotherapy academic and professional qualification to understand patient needs and support clinical coordination.Educational Requirement• Master’s Degree in Physiotherapy (MPT) or relevant advanced physiotherapy qualification.Important Remarks• This job posting has expired on Indeed, which suggests the recruitments may be closed or under review.• Applicants will be evaluated based on relevance of physiotherapy and coordination experience.• Knowledge of Hindi and local communication skills is preferred.Experience and SkillsExperience Required• 1–3 years of experience in patient care, healthcare coordination, or physiotherapy operations is preferred.Key Skills Expected• Strong communication and patient interaction skills• Good organisational and scheduling capabilities• Ability to coordinate with therapists and healthcare teams• Basic documentation and reporting skills• Patient-centric service attitudeAge Eligibility• Not specified in the job posting.Salary Insights• Salary depends on last drawn / candidate’s experience; not explicitly defined in the posting.• Benefit package includes health insurance and provident fund.Company OverviewPortea Medical is a healthcare provider focused on home care, physiotherapy and rehabilitation solutions across India. The company aims to deliver patient-centred care with integrated operations and support services. The role is based at the Domlur, Bengaluru location.FAQsIs fixed salary mentioned?No. Salary is dependent on previous experience and negotiation.Is this role remote?No – it is an in-person operational role in Bengaluru.What qualification is needed?MPT or equivalent advanced physiotherapy qualification.What type of experience is preferred?Experience in healthcare operations or patient coordination.What are benefits?Health insurance and Provident Fund.Application Tips• Update your CV highlighting physiotherapy experience and care coordination.• Mention language skills, especially communication in local languages like Hindi.• Provide examples of managing patient scheduling or clinic operations.• Prepare to discuss teamwork and patient service in interviews.• Apply through direct contact methods listed in the posting as it’s expired on Indeed.

Why This Role MattersThe Manager – Physiotherapy Centre role at Dr. Prachi Shah Arora’s Physiotherapy & Aquatic Rehab Centre is critical for ensuring smooth, high-quality patient experience and effective daily clinic operations in a multidisciplinary rehabilitation environment. This position plays a key part in patient satisfaction, staff coordination, and maintaining a well-organised clinical facility that supports recovery and therapeutic excellence.Leaders in this role support clinicians, reception staff, and administrative functions — ensuring that patients receive timely attention, that the clinic runs efficiently, and that quality standards in patient service and physiotherapy care are upheld. This role directly contributes to improving healthcare delivery within the facility and enhancing its reputation in the local community.Job DescriptionThe Manager – Physiotherapy Centre will be responsible for running day-to-day operations of the physiotherapy and aquatic rehab centre, ensuring seamless interaction with patients, doctors, and staff.This role includes supervising administrative tasks, coordinating schedules, maintaining clinic infrastructure and supplies, managing communication, and supporting a positive clinic atmosphere. The Manager is expected to be organised, professional, and patient-focused to ensure excellent service delivery.Key Features of the Role• Position: Manager – Physiotherapy Centre• Employment Type: Full-Time, Permanent• Location: Malad East, Mumbai, Maharashtra, India• Salary Range: ₹25,000 – ₹40,000 per month• Work Schedule: Monday to Saturday, 10-Hour shifts• Clinic: Physiotherapy & Aquatic Rehab CentreResponsibilities• Oversee daily operations of the physiotherapy centre• Greet and manage patients, doctors, and staff reception activities• Monitor patient and doctor appointment logs• Maintain clinic infrastructure, inventory of medical items and stationery• Ensure a positive and presentable clinic environment• Manage communication including calls and messages (WhatsApp when required)• Assist in maintaining progress sheets and patient case files• Coordinate Zoom / Google Meet setups for virtual consults when necessary• Collect patient feedback and resolve queries professionally• Lead and unite the team with patience and leadership qualitiesRequired QualificationCandidates must meet the essential educational and skill requirements to manage a physiotherapy centre effectively.Educational Requirement• Proficiency in Microsoft Excel and Google Sheets• Comfortable using Zoom / Google Meet for virtual communication• Good English communication skills (spoken and written)• Prior experience in a medical or clinic front desk role is a plusImportant Remarks• This is an in-person role requiring reliable commuting or relocation in Mumbai• Focus on organisation, professionalism, and patient interaction is expected• Experience in healthcare administration or clinic operations will be valuedExperience and SkillsExperience Required• Experience handling front desk, reception, or administrative responsibilities• Prior exposure to clinic or healthcare setting is advantageousKey Skills Expected• Strong organisational and communication skills• Patience and professionalism in patient interactions• Ability to manage clinic logistics and schedules• Skilled in basic software (Excel, Sheets, Zoom / Meet)• Team leadership and coordination abilitiesAge Eligibility• Not specified Salary Insights• ₹25,000 – ₹40,000 per month based on experience and skillsCompany OverviewDr. Prachi Shah Arora’s Physiotherapy & Aquatic Rehab Centre is a specialist rehabilitation facility located in Malad East, Mumbai. The clinic offers services in physiotherapy, aquatic therapy, sports rehab, and related therapeutic treatments. The centre focuses on delivering high-quality care and creating a supportive environment for both patients and staff.FAQsIs previous physiotherapy clinical experience required?Not mandatory, but relevant experience in admin or patient interaction is preferred.What software skills are needed?Comfort with Microsoft Excel, Google Sheets, and virtual meeting platforms like Zoom is expected.Is relocation required?The job requires being present in Malad East, Mumbai; relocation or commute should be arranged.What are working days?Monday to Saturday in a 10-hour shift schedule.How much does the role pay?Salary is between ₹25,000 – ₹40,000 per month.Application Tips• Highlight any healthcare or clinic admin experience in your CV• Demonstrate organisational and communication competence• Prepare examples of handling front-desk or customer interactions• Mention tech skills such as Excel and Zoom in applications• Apply early through Indeed before the position is filled

Why This Role MattersIn today’s pharmaceutical and research-driven environment, computerized systems are at the core of quality, compliance, data management, and regulatory reporting. Ensuring that these systems function accurately, securely, and in compliance with global regulatory expectations is critical for patient safety, product quality, and organizational credibility.The QA – Computer System Validation (CSV) role at B&S Group, Gowrie Research Pvt. Ltd., Vadodara plays a vital role in safeguarding data integrity and ensuring that all GxP computerized systems meet stringent regulatory standards such as 21 CFR Part 11 and other global compliance frameworks. This position directly impacts regulatory readiness, audit success, and operational excellence.By joining this role, professionals contribute to building a robust compliance culture while supporting innovation in R&D, analytical development, and project-driven pharmaceutical operations.Job DescriptionB&S Group, Gowrie Research Pvt. Ltd., Vadodara is conducting a Walk-In Drive for Women Professionals from 23rd to 27th February 2026, offering an opportunity in QA – Computer System Validation (CSV). The organization is seeking an experienced and technically strong M.Pharm professional with 7–10 years of relevant experience in computerized system validation within pharmaceutical or regulated environments.The selected candidate will be responsible for ensuring lifecycle validation, regulatory compliance, risk assessment, and documentation control for computerized systems used in Quality Assurance, R&D, Analytical Development Laboratory (ADL), and other regulated functions.This role requires a strong understanding of GxP requirements, regulatory guidelines, data integrity principles, and system validation methodologies. The position demands close coordination with cross-functional teams including IT, QA, regulatory, and user departments to ensure system compliance from implementation through ongoing operation.Key Features of the RoleOpportunity to lead validation of critical computerized systems in a regulated pharmaceutical environment.Direct exposure to regulatory compliance standards including GxP and 21 CFR Part 11.Involvement in R&D and special product development support systems.Participation in regulatory inspections, internal audits, and compliance improvement initiatives.Women-focused empowerment hiring initiative promoting leadership and technical excellence.Structured career progression within QA and regulatory compliance domains.Responsibilities RequiredLead and manage validation activities for computerized systems across departments including Quality, R&D, Analytical Development, and Project Management.Prepare, review, and approve validation documentation such as User Requirement Specifications (URS), Functional Specifications (FS), Design Specifications (DS), Risk Assessments, Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Validation Summary Reports.Ensure compliance of all computerized systems with applicable regulatory requirements including GxP guidelines and 21 CFR Part 11 standards for electronic records and electronic signatures.Conduct risk-based assessments to identify potential compliance gaps and recommend corrective and preventive actions.Review vendor documentation, system configuration details, and qualification packages to ensure regulatory adequacy before system deployment.Monitor and evaluate change control activities related to system upgrades, patches, software enhancements, and configuration changes. Ensure appropriate impact assessment and revalidation activities are conducted.Support regulatory inspections and internal audits by providing complete validation documentation and addressing compliance-related queries.Ensure implementation of robust data integrity controls including audit trail reviews, user access management, password policies, backup and recovery systems, and periodic system reviews.Collaborate with IT and software vendors to ensure secure system architecture, validation compliance, and continuous performance monitoring.Maintain proper documentation practices, version control, and archival procedures in alignment with Quality Management System (QMS) requirements.Provide training and awareness sessions to cross-functional teams regarding CSV lifecycle approach, data integrity expectations, and regulatory updates.Participate in continuous improvement initiatives to enhance validation efficiency, documentation standards, and compliance readiness.QualificationsCandidates should possess a strong technical and regulatory background with demonstrated experience in Computer System Validation within pharmaceutical or regulated environments.Educational Requirements:Master of Pharmacy (M.Pharm) from a recognized university or institution.Experience and Skills:7–10 years of relevant experience in QA – Computer System Validation within pharmaceutical, biotech, or regulated research environments.In-depth knowledge of GxP requirements and 21 CFR Part 11 compliance.Strong understanding of lifecycle-based validation approaches and risk-based methodologies.Hands-on experience in preparation and execution of IQ, OQ, PQ protocols.Experience handling regulatory audits and inspection readiness activities.Strong documentation, analytical, and review skills.Excellent coordination and communication skills to manage cross-functional teams.High attention to detail and ability to manage multiple validation projects simultaneously.Salary InsightsCompensation will be competitive and aligned with industry standards for professionals with 7–10 years of CSV experience. Salary packages typically depend on candidate expertise, regulatory exposure, audit-handling capability, and leadership responsibilities.Additional benefits may include:Performance-based incentivesProfessional growth opportunities in R&D and regulatory domainsExposure to special product development projectsWomen-focused empowerment initiative supportStructured performance evaluation and career progression pathwaysCompany OverviewB&S Group, Gowrie Research Pvt. Ltd., Vadodara is a reputed pharmaceutical research and development organization engaged in formulation development, analytical research, regulatory documentation, and quality compliance operations.The organization emphasizes regulatory excellence, innovation-driven research, and structured Quality Management Systems. With strong focus on R&D, compliance, and specialized product development, the company provides professionals with an environment that supports technical growth, regulatory exposure, and leadership development.Through its Women Professionals Walk-In Drive initiative, the organization aims to promote diversity, technical excellence, and inclusive leadership within the pharmaceutical and research ecosystem.FAQsWho is eligible to apply for this position?Women professionals with M.Pharm qualification and 7–10 years of relevant CSV experience in regulated pharmaceutical environments are eligible.Is prior audit-handling experience required?Yes, experience in supporting regulatory inspections and internal audits is highly preferred.What type of systems will be validated?Computerized systems used in Quality Assurance, R&D, Analytical Development, and related regulated functions.Is knowledge of 21 CFR Part 11 mandatory?Yes, strong understanding of 21 CFR Part 11 and data integrity principles is essential for this role.What is the selection process?Candidates can attend the walk-in interview between 23rd to 27th February 2026 with updated resume and educational documents.Application TipsEnsure your resume clearly highlights CSV projects handled, validation documentation prepared, and audit exposure.Mention specific experience related to 21 CFR Part 11 compliance and GxP systems.Include examples of risk assessments conducted and change control management handled.Carry all relevant educational certificates, experience letters, and identification documents during the walk-in.Prepare to discuss real-time validation scenarios, data integrity controls, and regulatory inspection experiences confidently.

Why This Role MattersEffective project management is essential in pharmaceutical R&D to ensure that development timelines, regulatory submissions, and cross-functional activities remain aligned. Delays in coordination or lifecycle tracking can directly impact product launches, regulatory approvals, and business outcomes.This Walk-In Drive, organized by Gowrie Research Pvt. Ltd. under B&S Group, provides an excellent opportunity for women professionals to build careers in pharmaceutical project management. The role is ideal for candidates who want exposure to regulated environments, structured development processes, and cross-functional collaboration within R&D and regulatory domains.Professionals joining this function will act as a bridge between formulation, analytical, QA, and other departments to ensure smooth execution of projects from initiation to completion.Job DescriptionB&S Group – Gowrie Research Pvt. Ltd., Vadodara, is conducting a Walk-In Drive for Women Professionals from 23rd to 27th February 2026. Among the open roles, the organization is hiring for Project Management positions to support pharmaceutical R&D and regulatory-driven projects.The selected candidates will be responsible for tracking project lifecycles, coordinating cross-functional teams, managing timelines, and preparing progress reports. The role requires strong organizational skills, communication ability, and structured documentation practices.Key Features of the Role• Involvement in end-to-end pharmaceutical project lifecycle management• Cross-functional exposure across F&D, ADL, QA, and regulatory teams• Opportunity to work in a structured R&D environment• High visibility coordination role supporting leadership• Women-focused hiring initiative encouraging professional growth• Strong foundation for future leadership roles in project managementResponsibilities RequiredProject Lifecycle Tracking• Monitor project timelines from initiation through completion• Track key milestones, deliverables, and dependencies• Maintain project trackers and status dashboards• Identify potential delays and escalate risks proactively• Ensure adherence to approved development timelinesCross-Functional Coordination• Coordinate between Formulation & Development, Analytical Development, QA, and other departments• Schedule and facilitate project review meetings• Communicate updates and align stakeholders on priorities• Support resolution of inter-departmental challenges• Ensure smooth flow of information across teamsTimeline Management & Reporting• Prepare periodic project progress reports• Develop executive summaries for leadership review• Track resource allocation and project status updates• Maintain documentation related to project activities• Support compliance with internal SOPs and regulatory expectationsSenior Role Responsibilities• Lead coordination of multiple projects simultaneously• Guide junior team members or trainees• Contribute to strategic planning discussions• Support regulatory submission timelines• Improve project management processes for efficiencyTrainee Role Responsibilities• Assist in maintaining trackers and documentation• Support coordination meetings and follow-ups• Learn project lifecycle management processes• Participate in data collection and reporting activities• Gain exposure to R&D and regulatory project workflowsQualificationsCandidates should demonstrate strong organizational capability, structured thinking, and the ability to manage multiple stakeholders effectively. The role requires attention to detail and accountability in managing timelines and documentation.For senior-level roles, prior experience in handling pharmaceutical R&D projects is essential.Educational Requirements• Master's degree in Pharmacy (M.Pharm) (Mandatory for both Senior and Trainee roles)• Specialization in Pharmaceutics, Pharmaceutical Analysis, or related field preferredExperience and SkillsExperience• 3–5 years for Senior Officer / Executive role• 0–1 year for Trainee role• Exposure to pharmaceutical R&D or regulatory environment preferredTechnical Skills• Strong understanding of project lifecycle management• Knowledge of pharmaceutical development processes• Familiarity with regulatory timelines and compliance requirements• Proficiency in MS Excel and PowerPoint for reporting• Ability to manage structured documentation and trackersBehavioral Skills• Strong communication and interpersonal skills• Excellent time management and prioritization ability• Problem-solving mindset• Attention to detail and accuracy• Ability to work collaboratively across departments• Leadership capability for senior-level roleSalary Insights• Estimated salary range (Senior Role): ₹5 LPA – ₹8 LPA• Estimated salary range (Trainee Role): ₹2.5 LPA – ₹4 LPA• Compensation depends on experience and project exposure• Performance-based incentives may be applicableAdditional Benefits• Performance-based incentives• Professional growth in R&D and regulatory domains• Exposure to special product development initiatives• Women-focused empowerment hiring initiative• Structured learning environment for traineesCompany OverviewGowrie Research Pvt. Ltd., part of B&S Group, is a pharmaceutical research-driven organization engaged in formulation development, analytical research, quality systems, and regulatory compliance activities.Based in Vadodara, the organization emphasizes innovation, regulatory excellence, and operational efficiency. It provides strong career progression opportunities in R&D, QA, analytical sciences, and project management functions.Walk-In & Application ProcessWalk-In Dates: 23rd to 27th February 2026Location: VadodaraInterested candidates should• Attend the walk-in interview during the specified dates• Carry updated resume and educational documents• Arrive early due to limited vacanciesFAQsIs this walk-in drive only for women professionals?Yes, this is a dedicated hiring initiative for women professionals.Is experience mandatory for the Trainee role?No, fresh M.Pharm graduates with strong coordination skills can apply.Does the role involve technical laboratory work?No, this role focuses on project coordination and lifecycle tracking.What career growth can be expected?Candidates can progress to Project Manager, Program Manager, or R&D Leadership roles.Is pharmaceutical industry experience required for the senior role?Yes, 3–5 years of relevant experience is required for the Senior Officer / Executive position.Application Tips• Highlight project coordination or internship experience• Mention exposure to R&D or regulatory timelines• Showcase Excel-based tracking or reporting work• Emphasize communication and stakeholder management skills• Carry all educational and experience documents for verificationThis walk-in opportunity offers a strong platform for women professionals seeking growth in pharmaceutical project management and cross-functional R&D coordination roles.

Why This Role MattersIn today’s fast-evolving pharmaceutical landscape, business decisions must be driven by accurate data, field intelligence, and strong cross-functional collaboration. Strategy alone is not enough — it must be validated on the ground, aligned with therapy objectives, and continuously refined based on performance insights.This role plays a crucial part in connecting central strategy teams with field execution. By analyzing business data, coordinating with leadership stakeholders, and validating initiatives at the field level, the position ensures that commercial strategies are both practical and performance-oriented.For early-career professionals, this is a high-impact opportunity to work closely with senior leadership, contribute to business growth initiatives, and build a strong foundation in analytics, stakeholder management, and strategic execution within a reputed pharmaceutical organization like Lupin Limited.Job DescriptionThis position supports strategic and field-driven business initiatives by combining analytics, coordination, reporting, and field validation activities. The role requires a highly analytical, detail-oriented, and proactive individual who can translate data into actionable insights while effectively managing multiple stakeholders across functions.The selected candidate will work closely with marketing leadership, business unit heads, and field teams to ensure that therapy-level objectives are met, business projects are tracked effectively, and performance gaps are identified and addressed promptly.The role demands strong ownership, structured thinking, and the ability to operate in a dynamic business environment where priorities may evolve based on market conditions.Key Features of the Role• High visibility exposure to strategic business initiatives• Direct collaboration with Marketing Head, BU Head, and field leadership• Opportunity to develop advanced Excel dashboards and analytics models• Monthly field visits to validate strategy implementation• Exposure to therapy-level planning and commercial excellence practices• Strong foundation for career growth in business analytics, marketing strategy, and commercial operations• Hands-on involvement in performance benchmarking and competitor analysisResponsibilities RequiredData Analysis & Business Insights• Analyze large and complex datasets to identify trends, patterns, and business opportunities• Generate actionable insights to support therapy-level and business unit decision-making• Perform data cleaning, validation, and ongoing database maintenance• Develop automated dashboards and trackers to monitor KPIs such as sales growth, market share, productivity, and target achievement• Conduct detailed performance comparisons across regions, territories, and therapy segments• Identify underperforming areas and recommend corrective strategies• Support leadership with ad-hoc analysis and scenario modeling• Ensure data accuracy and consistency across multiple reporting systemsStakeholder Coordination & Alignment• Understand therapy-level business objectives and align project deliverables accordingly• Work closely with Marketing Head and Business Unit Head to support strategic initiatives• Coordinate with cross-functional stakeholders including sales, marketing, finance, and operations• Organize and participate in review meetings with head office and field leadership• Track action items, follow up on deliverables, and ensure timely completion of projects• Facilitate communication between central teams and field representatives• Support implementation of new processes and performance frameworksField Strategy Validation• Conduct monthly field visits to understand real-time execution models• Observe sales operations, territory management, and customer engagement practices• Validate whether central strategies are being implemented effectively• Gather feedback from field teams regarding challenges and improvement areas• Provide structured feedback to leadership based on field observations• Recommend process enhancements to improve execution efficiency• Bridge the gap between planning and ground realitiesReporting & Leadership Presentations• Prepare concise, insight-driven reports for leadership review• Develop structured PowerPoint presentations with clear storytelling and data visualization• Build executive dashboards using Advanced Excel• Convert analytical findings into actionable business recommendations• Maintain trackers to monitor progress of strategic initiatives• Present findings confidently during leadership review meetingsQualificationsThe ideal candidate should possess strong analytical capabilities, structured thinking ability, and the confidence to interact with senior stakeholders. The role requires someone who is comfortable working with data, capable of handling ambiguity, and eager to learn about pharmaceutical business dynamics.A high level of accountability and initiative is essential, as the position involves independent ownership of projects and deliverables.Educational Requirements• Graduation in Science or Engineering• Post Graduation in Business Administration (MBA preferred)Candidates with strong academic backgrounds in analytical disciplines will be highly valued.Experience and SkillsExperience• 0–2 years of relevant experience• Freshers with strong analytical aptitude are encouraged to apply• Internship experience in analytics, strategy, or commercial functions is an advantageTechnical Skills• Advanced Excel proficiency (Pivot Tables, VLOOKUP/XLOOKUP, Index-Match, Dashboards, Data Modeling)• Strong PowerPoint skills (visual storytelling, structured slides, executive summaries)• Data interpretation and analytical thinking capability• Ability to handle large datasets efficientlyCore Competencies• Strategic Agility – Ability to adapt business insights to changing priorities• Customer Centricity – Understanding market and customer dynamics• Process Excellence – Focus on improving efficiency and accuracy• Result Orientation – Commitment to delivering measurable outcomes• Stakeholder Management – Effective coordination across teams• Collaboration – Strong team-oriented approach• Developing Talent – Openness to feedback and continuous learning• Innovation & Creativity – Ability to suggest new analytical approachesSalary Insights• Estimated compensation range: ₹4.5 LPA – ₹7 LPA• MBA candidates with strong analytical skills may command higher packages• Performance-based increments and internal growth opportunities available• Exposure to leadership increases long-term earning potentialCompany OverviewLupin Limited is one of India’s leading pharmaceutical companies with a strong global presence across generics, branded formulations, and specialty segments. Known for its innovation-driven approach and high-quality manufacturing standards, Lupin operates in multiple international markets and maintains a strong focus on patient-centric healthcare solutions.The organization offers dynamic career pathways in marketing, commercial excellence, analytics, and strategic leadership functions, making it an excellent platform for early-career professionals to build a strong corporate foundation.FAQsIs this role suitable for fresh graduates?Yes, candidates with strong analytical skills and learning agility are encouraged to apply.Is travel involved in this role?Yes, monthly field visits are part of the role to validate strategy implementation.Is this a core sales position?No, this is a strategic analytics and coordination role supporting business units.What career growth can be expected?This role can lead to opportunities in Commercial Excellence, Marketing Strategy, Business Analytics, and BU Leadership roles.Is MBA mandatory?MBA is preferred but not mandatory if the candidate demonstrates strong analytical and presentation skills.Application Tips• Highlight Excel dashboard projects, certifications, or academic analytics work• Mention internships or projects related to business strategy or data analysis• Showcase structured PowerPoint presentations if available• Demonstrate problem-solving ability with measurable outcomes• Emphasize communication skills and stakeholder coordination experience• Quantify achievements wherever possible

Why This Role MattersThe Safety Submissions Specialist plays a critical role in global clinical trial safety reporting. With increasing regulatory scrutiny from authorities such as the FDA, EMA, and MHRA, timely and accurate submission of safety reports is essential to maintain compliance and protect patient safety. This role directly supports regulatory adherence, audit readiness, and risk mitigation in global clinical trials. It is a strategic opportunity for professionals looking to strengthen their expertise in pharmacovigilance operations and international safety reporting.Job DescriptionThe Safety Submissions Specialist is responsible for reviewing, preparing, and transmitting Individual Case Safety Reports (ICSRs) and other regulatory safety documents to global health authorities, affiliates, and business partners. The role requires strong knowledge of international safety regulations, electronic submission systems, and pharmacovigilance databases.Key Features of the Role• Direct exposure to global clinical trial safety submissions• Hands-on experience with ICSR electronic transmission and regulatory portals• Interaction with international regulatory authorities• Involvement in TMF compliance and Safety Reporting Plans• Growth opportunity in drug safety and regulatory compliance• Work within FDA, EU, UK, and ICH safety frameworksResponsibilities Required• Monitor Drug Safety Inbox for acknowledgements and expedited reporting confirmations• Generate final clinical trial regulatory reports (CIOMS I, MedWatch 3500A, XML formats)• Review and transmit ICSR submissions (paper and electronic formats)• Prepare and distribute Investigator Safety Letters• Perform SAE case closure and electronic filing• Conduct SAE reconciliation and distribute SUSAR Gap Packs• Manage expedited reporting deviations and support CAPA documentation• Maintain submission trackers, compliance logs, and reporting metrics• Support development and updates of Safety Reporting Plans• Monitor global regulatory intelligence updates• Ensure documentation compliance within TMF and PSMF• Maintain adherence to GCP, ICH, FDA, EU GVP, and MHRA guidelinesQualificationsCandidates must have strong operational knowledge of clinical trial safety reporting and global pharmacovigilance regulations. Experience working in Pharma or CRO environments is preferred.Educational Requirements• Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related field• B.Pharm / M.Pharm / PharmD preferred• Pharmacovigilance certification is an added advantageExperience and SkillsExperience:• Minimum 2 years in clinical trial drug safety or pharmacovigilance• Experience in Pharma or CRO settingTechnical Skills:• Knowledge of FDA safety reporting requirements• Understanding of ICH guidelines (E2A, E2B, E6)• Familiarity with EU Pharmacovigilance regulations and GVP modules• Hands-on experience with ARGUS Safety Database• Experience with EMA EudraVigilance portal• Experience with UK MHRA reporting systems• Familiarity with other global electronic submission portalsFunctional Skills:• Strong attention to detail• Excellent documentation and compliance practices• Ability to manage multiple submissions within strict timelines• Strong coordination and communication skills• Analytical mindset for reconciliation and deviation handlingSalary Insights• Estimated salary range in Bengaluru: ₹5.5 LPA – ₹10 LPA (for 2–4 years experience)• Compensation depends on ARGUS expertise, regulatory exposure, and CRO experience• Additional benefits may include insurance, performance bonuses, and career development programsCompany OverviewPrecision Medicine Group is a global clinical research and life sciences services organization supporting pharmaceutical, biotech, and medical device companies. The company specializes in clinical development, pharmacovigilance, and regulatory compliance services, helping sponsors accelerate drug development while maintaining global compliance standards.FAQsIs this role focused on clinical trials or post-marketing safety?This role primarily supports clinical trial safety reporting.Is ARGUS experience mandatory?Hands-on ARGUS experience is strongly preferred.Is this a remote role?No, this is an on-site position in Bengaluru.Does the role involve global submissions?Yes, submissions may involve FDA, EMA, MHRA, and other authorities.Is CRO experience required?CRO experience is preferred but not mandatory.Application Tips• Clearly highlight ARGUS database experience in your CV• Mention exposure to ICSR submissions (E2B, XML, CIOMS, MedWatch)• Include examples of expedited reporting and SUSAR reconciliation• Demonstrate familiarity with FDA, EU, and MHRA regulations• Quantify your experience (e.g., number of submissions handled per month)• Emphasize audit readiness and compliance accuracy experience

Why This Role MattersThe Clinical Research Coordinator (CRC) plays a pivotal role in advancing global healthcare research. By managing clinical trials from patient screening to regulatory documentation, CRCs ensure that medical studies are conducted efficiently, safely, and in compliance with international standards. This position directly impacts the quality of clinical outcomes, the integrity of research data, and the well-being of study participants.Working in a remote capacity in India, CRCs at MaximaTek support international sponsors and research teams, bridging gaps between study sites, regulatory bodies, and patients. Their work not only contributes to the success of global clinical trials but also promotes the development of new treatments and therapies that improve patient care worldwide.For professionals in the clinical research industry, this role offers a unique combination of operational oversight, patient engagement, and regulatory compliance. The CRC’s meticulous approach ensures studies maintain credibility while protecting participant safety, making it an essential position for both the research team and the broader healthcare community.Job DescriptionThe Clinical Research Coordinator at MaximaTek is responsible for managing all aspects of clinical trial operations for global studies. This remote position offers flexible engagement models, including part-time, full-time, and freelance work in a US shift schedule. The role requires extensive experience in clinical research coordination, strong knowledge of regulatory requirements, and expertise in patient-centric operations.Key Responsibilities Include:Managing study subjects, including screening, enrollment, and treatment, in accordance with trial protocols.Conducting eligibility assessments and obtaining informed consent.Ensuring strict adherence to ICH-GCP guidelines and internal standard operating procedures (SOPs).Acting as a liaison between sponsors, CROs, and research sites.Supporting sample collection, processing, and storage activities.Assisting with regulatory submissions and protocol review processes.Maintaining essential documents, regulatory binders, and clinical trial databases.Supporting monitoring visits and ensuring audit readiness.Providing cross-functional support for short-term or ad-hoc research projects.This role demands operational oversight, regulatory compliance, and effective coordination across multiple teams to ensure clinical trials run smoothly and data integrity is maintained.ResponsibilitiesThe Clinical Research Coordinator manages day-to-day operations of clinical trials, ensuring patient safety, protocol compliance, and regulatory documentation are maintained to the highest standard. Daily work involves patient engagement, documentation, and collaboration with cross-functional teams.Responsibilities include:Patient Management: Conduct screening, enrollment, and treatment, ensuring adherence to protocols and patient safety standards.Regulatory Compliance: Maintain trial documentation, regulatory binders, and assist with submissions to ensure trials meet ICH-GCP and sponsor requirements.Coordination with Sponsors & CROs: Serve as a communication bridge between research sites and external stakeholders, facilitating smooth trial execution.Sample Handling: Oversee collection, processing, and storage of clinical samples following SOPs and safety guidelines.Monitoring & Audit Support: Prepare for monitoring visits, audits, and inspections by maintaining accurate trial records and readiness protocols.Cross-Functional Assistance: Support short-term projects, protocol amendments, and other operational initiatives as needed.Required QualificationsThe ideal candidate for the Clinical Research Coordinator role will have a solid educational background in life sciences or related fields and extensive hands-on experience in clinical trial management.Education & Experience:Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field.Minimum 7+ years of experience as a Clinical Research Coordinator.Experience in US-based clinical trials is preferred.Prior exposure to regulatory submissions, protocol reviews, and monitoring support.Key Skills & Competencies:Strong written and verbal communication abilities for global team coordination.Excellent organizational skills and meticulous documentation practices.Knowledge of clinical safety protocols, human research ethics, and regulatory compliance.Ability to work independently in a remote environment while maintaining effective collaboration across teams.Candidates must also comply with mandatory research training and medical surveillance requirements, ensuring safe and compliant clinical trial operations.Salary InsightsThe Clinical Research Coordinator role at MaximaTek offers a competitive salary range of approximately ₹8,00,000 – ₹14,00,000 per annum, depending on experience, engagement type, and responsibilities.Employment Type Impact: Part-time, full-time, or freelance arrangements may influence the annual pay scale and benefits.Experience & Expertise: Professionals with prior US-based trial exposure or regulatory experience may command higher compensation.Additional Benefits: Remote working flexibility, exposure to global clinical research projects, and opportunities for performance-based growth.Salary structures in clinical research can vary based on industry standards, trial complexity, and professional certifications, making expertise and proven track records valuable for long-term earning potential.Career Growth PathThe Clinical Research Coordinator role offers extensive career progression in global clinical research. Professionals can develop expertise in trial coordination, regulatory compliance, and patient engagement, opening pathways to leadership roles.Entry-Level Progression:Master operational tasks, such as patient management, documentation, and monitoring support.Gain familiarity with regulatory requirements and study protocols.Mid-Level Advancement:Take responsibility for larger trials or multiple studies.Support protocol development, regulatory submissions, and team mentoring.Senior-Level Opportunities:Lead clinical trial operations, manage CRC teams, or oversee regulatory compliance for multinational studies.Contribute to strategic planning and clinical operations improvement initiatives.Skills & Certifications That Support Growth:Advanced clinical research certifications and courses in regulatory compliance.Strong project management, data analysis, and leadership skills.Continuous learning in patient-centric care, clinical trial innovations, and global regulatory standards.Company OverviewMaximaTek is a private organization operating in the clinical research and clinical trials industry, providing remote coordination support for global studies. With a focus on patient-centric, decentralized trials, MaximaTek connects professionals with international sponsors and research sites, fostering innovation and compliance in clinical research.Work Culture: Flexible, remote-first environment with US shift schedules. Encourages collaboration, adherence to global standards, and continuous learning.Reputation: Recognized for supporting complex clinical trials while maintaining rigorous compliance and patient safety standards.Role Integration: The Clinical Research Coordinator is essential to MaximaTek’s operations, ensuring trial efficiency, high-quality data, and participant safety.FAQsWhat qualifications are required for this role?A Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or related field, with 7+ years of CRC experience, is essential. US-based trial experience is preferred.What is the salary range?Approximately ₹8,00,000 – ₹14,00,000 per year, depending on experience, employment type, and responsibilities.What career growth opportunities exist?Entry-level CRCs can progress to senior trial management, regulatory coordination, or leadership roles in clinical operations.What documents are required to apply?Updated resume, cover letter, certifications, and proof of mandatory research training or medical surveillance compliance.What is the work environment like?Fully remote from India, working in US shift schedules, collaborating with global sponsors, research sites, and cross-functional teams.How does one apply?Submit your resume and cover letter via email to the provided contact. Early applications are recommended due to high interest.Application TipsTo enhance chances of selection for the Clinical Research Coordinator role:Ensure all eligibility criteria, including educational qualifications and CRC experience, are clearly met.Prepare a detailed resume highlighting experience in patient management, regulatory submissions, and clinical trial coordination.Include specific examples of managing global trials, US-based study protocols, or regulatory compliance tasks.Tailor your cover letter to demonstrate familiarity with decentralized trial operations and US shift work.Provide all required documents, including proof of certifications and mandatory research training.Emphasize communication, organizational skills, and ability to work independently in a remote environment.Ensure applications are error-free, professional, and submitted early to account for high competition.

Serve as a scientific peer-to-peer resource to disease experts and healthcare professionals. Must have PhD, PharmD, or MD.

Roles and Responsibilities:• Manage day-to-day operations of the physiotherapy and aquatic rehabilitation centre.• Monitor and maintain patient and doctor logs.• Handle patient relationship management and collect feedback regularly.• Oversee maintenance of centre infrastructure, decor, and ensure a positive clinic environment.• Manage inventory of medical supplies and stationery.• Lead, coordinate, and unify the team as a team leader.• Set up and manage Zoom and Google Meet sessions for virtual consultations, especially for international clients (IST).• Attend and respond to phone calls and WhatsApp messages when required.• Assist doctors in maintaining progress sheets and patient case files.• Greet and guide patients with professionalism, politeness, and clarity.Qualification:• Graduate in any discipline (preferred).Experience:• Prior experience in medical or clinic front desk/administration roles preferred.• Experience in team handling and operational management is an advantage.Skills:• Proficiency in Microsoft Excel, Microsoft Word, and Google Sheets.• Comfortable using Zoom and Google Meet platforms.• Good command of English (spoken and written).• Strong organizational and communication skills.• Presentable, patient-focused, and professional attitude.• Leadership and team coordination abilities.Benefits:• 33 paid leaves annually (including Birthday Leave, December 31 & January 1 off).• Performance-based bonus.• Free massages, gym facility, swimming training, and physiotherapy treatment.• Supportive and well-established team environment.About the Company:Dr. Prachi Shah Arora's Physiotherapy & Aquatic Centre is a leading rehabilitation centre in Mumbai known for excellence in sports, aquatic, neuro, geriatric, and paediatric physiotherapy. The centre emphasizes innovative care, patient satisfaction, and a collaborative work culture.

Roles & Responsibilities• Support execution and monitoring of project activities under DBT Nidan Kendra• Assist in clinical/research data collection, analysis, and documentation• Coordinate with investigators, clinical staff, and research teams• Ensure compliance with institutional and regulatory guidelines• Prepare project reports and assist in submission of progress updates• Support laboratory/clinical procedures as per project requirements• Maintain proper documentation and ensure audit readinessQualification• B.E. / MD / MS / Pharm D / Postgraduate degree (relevant field)Experience• Relevant experience in clinical research, biomedical projects, or healthcare settings preferredAge Limit• Minimum: 21 Years• Maximum: 45 Years• Age relaxation as per organizational normsSelection Process• Written Test• InterviewImportant Dates• Starting Date: 19-02-2026• Closing Date: 27-02-2026AddressDBT Nidan Kendra, Dept. of Obstetrics & Gynaecology, JNIMCH, AMU, Aligarh, IndiaSkills • Knowledge of clinical research methodologies and biomedical project execution• Strong documentation and report writing skills• Familiarity with regulatory and ethical guidelines• Data management and analytical abilities• Effective communication and coordination skills• Time management and ability to meet project deadlines• Proficiency in MS Office and basic research toolsAbout the OrganizationAligarh Muslim University is a renowned central university recognized for excellence in education, medical research, and healthcare innovation in India.Official Notification Click Here

Roles and Responsibilities:• Manage patient coordination and ensure smooth physiotherapy service delivery.• Schedule and manage physiotherapy appointments efficiently.• Coordinate with physiotherapists for workload planning and case allocation.• Conduct patient follow-ups and track treatment progress.• Handle documentation, consent forms, and compliance requirements.• Address patient queries and manage feedback professionally.• Prepare basic operational reports and coordinate with the operations team.Qualification:• Master of Physiotherapy (MPT)Experience:• 1–3 years’ experience in patient care or healthcare coordinationSkills:• Strong patient interaction and communication skills• Scheduling and coordination abilities• Documentation and reporting skills• Hindi language proficiency (mandatory)• Organisational and multitasking abilitiesBenefits:• Health Insurance• Provident FundAbout the Company:Portea Medical is a leading home healthcare provider in India, offering medical, nursing, physiotherapy, and rehabilitation services at patients’ homes. The organisation focuses on delivering accessible, quality healthcare solutions with a strong operations and coordination framework to ensure patient satisfaction and clinical excellence.