Pharmacy Jobs in Mumbai

Why This Role MattersThe Senior Purchasing Manager plays a critical role in ensuring the continuous supply of raw materials and packaging materials required for pharmaceutical manufacturing. By developing procurement strategies, managing supplier relationships, and optimizing costs, the role supports efficient production operations while maintaining compliance with pharmaceutical regulatory and quality standards.Job DescriptionRusan Pharma Ltd is hiring a Senior Manager – Purchase for a full-time on-site position in Kandivali, Mumbai. The role involves leading procurement strategies for raw materials and packaging materials used in formulation manufacturing, managing supplier relationships, ensuring regulatory compliance, and supporting efficient supply chain operations.Key Features of the Role• Position: Senior Manager – Purchase• Company: Rusan Pharma Ltd• Location: Kandivali, Mumbai, Maharashtra, India• Employment Type: Full-Time• Workplace Type: On-site• Experience: Minimum 10 years in procurement within pharmaceutical organizations• Department: PurchaseResponsibilities• Develop and implement procurement strategies for raw materials such as APIs and excipients, and packaging materials• Lead strategic sourcing initiatives and negotiate supplier contracts to optimize costs• Identify value engineering opportunities and improve procurement efficiency• Establish alternate sourcing strategies to strengthen supply chain resilience• Ensure procurement activities comply with pharmaceutical regulatory and quality standards• Identify and mitigate supply chain risks to maintain uninterrupted material availability• Maintain procurement documentation aligned with regulatory and audit requirements• Coordinate with Quality Assurance and Regulatory teams for supplier qualification and compliance• Align procurement planning with production schedules and inventory optimization goals• Monitor procurement KPIs such as cost savings, supplier reliability, and lead time adherence• Implement continuous improvement initiatives to enhance procurement processes• Collaborate with manufacturing, supply chain, R&D, quality, and finance teams• Manage vendor relationships, supplier performance, and strategic partnershipsRequired Qualification• Graduate in Science or Pharmacy• MBA or PGDM in Materials Management or Supply Chain Management (preferred)Important Requirements• Minimum 10 years of progressive experience in procurement within pharmaceutical manufacturing• Experience in sourcing raw materials and packaging materials for formulations• Strong knowledge of pharmaceutical procurement compliance and regulatory standards• Experience in supplier management and contract negotiations• SAP ERP experience for procurement and material management• Strong analytical and stakeholder management skillsWhat We Offer• Opportunity to work with an established pharmaceutical manufacturing company• Leadership role in procurement and supply chain strategy• Exposure to strategic sourcing and vendor development initiatives• Collaborative cross-functional work environmentExperience and Skills• Strategic sourcing and procurement planning• Vendor development and contract negotiation• Supply chain risk management• Cost optimization and procurement analytics• SAP ERP procurement systems• Data analysis and MIS reportingSalary Insights• Salary details are not specified in the job listing• Compensation may vary depending on experience, leadership responsibilities, and company policiesCompany OverviewRusan Pharma Ltd is a pharmaceutical company specializing in the development and manufacturing of formulations and active pharmaceutical ingredients. The company operates globally and focuses on delivering high-quality pharmaceutical products while maintaining strong regulatory compliance and manufacturing standards.FAQsWhat qualification is required for this role?Candidates must have a degree in Science or Pharmacy. An MBA or PGDM in Materials Management or Supply Chain Management is preferred.How much experience is required?The role requires a minimum of 10 years of procurement experience in pharmaceutical organizations.What are the key responsibilities in this role?The manager will oversee procurement strategies, vendor management, supply chain risk mitigation, and procurement process improvements.Where is the job located?The job is located in Kandivali, Mumbai, Maharashtra, India.Application Tips• Highlight your procurement and sourcing experience in pharmaceutical manufacturing• Mention experience with SAP ERP and procurement systems• Include vendor management and contract negotiation achievements• Emphasize supply chain risk management and cost optimization strategies• Demonstrate leadership experience in procurement operationsJ

Why This Role MattersClinical research plays a fundamental role in the development of new medicines, medical devices, and treatment strategies. Before a drug or therapy can be approved for patient use, it must undergo extensive clinical trials to evaluate its safety, efficacy, and overall therapeutic benefit. Clinical Research Associates (CRAs) are key professionals responsible for ensuring that these trials are conducted according to strict regulatory and ethical standards.The role of a Clinical Research Associate is critical in maintaining the quality and integrity of clinical trial data. CRAs act as the bridge between sponsors, research sites, investigators, and regulatory authorities. Their primary responsibility is to monitor clinical trial sites, verify data accuracy, and ensure compliance with international guidelines such as ICH-GCP.In modern clinical research, accurate documentation, proper site monitoring, and data verification are essential to ensure that clinical trial results are reliable and acceptable to regulatory authorities. CRAs ensure that study protocols are followed correctly, participant safety is maintained, and all clinical activities adhere to regulatory requirements.This role is especially valuable for professionals seeking a long-term career in clinical trials, contract research organizations (CROs), and pharmaceutical development. By gaining experience in monitoring, regulatory compliance, and clinical trial management, CRAs can build a strong career path in the global healthcare and pharmaceutical industry.Job DescriptionAnaZeal Analyticals and Research Pvt. Ltd. is hiring Clinical Research Associates to support clinical trial monitoring and site management activities. The role requires professionals who can ensure proper execution of clinical trials while maintaining compliance with regulatory standards and Good Clinical Practice guidelines.As a Clinical Research Associate, the selected candidate will be responsible for conducting site monitoring visits, reviewing clinical documentation, and verifying data accuracy through Source Data Verification processes. This includes ensuring that data recorded in electronic case report forms accurately reflects information recorded in source documents.The role also involves coordinating with investigators, sponsors, and clinical trial teams to ensure smooth study operations. CRAs are expected to monitor trial progress, identify potential issues, and provide solutions to maintain compliance and study timelines.Professionals in this role must maintain detailed monitoring reports, track regulatory documents, and support audit readiness. Ensuring that clinical trial documentation is complete and compliant is a key responsibility of the position.The job may require travel to clinical trial sites for monitoring visits, investigator meetings, and compliance assessments. Strong organizational skills, attention to detail, and effective communication abilities are essential to succeed in this position.Key Features of the Role:• Opportunity to work in a Clinical Research Organization (CRO) environment• Hands-on exposure to clinical trial monitoring and site management• Experience working with ICH-GCP regulatory guidelines• Direct interaction with investigators, sponsors, and clinical research teams• Field-based experience in real-world clinical trial environments• Career growth opportunities in clinical research and pharmaceutical developmentResponsibilities• Conduct site monitoring visits to ensure clinical trials are conducted according to protocol requirements.• Perform Source Data Verification (SDV) to confirm accuracy of clinical trial data.• Review study documentation including informed consent forms and regulatory files.• Ensure compliance with ICH-GCP guidelines and regulatory standards.• Coordinate with investigators, sponsors, and study teams to support clinical trial operations.• Submit monitoring visit reports within required timelines.• Identify site-related issues and work with the study team to resolve them.• Track study progress and ensure adherence to study protocols.• Review electronic Case Report Forms (eCRF) for completeness and accuracy.• Maintain proper documentation for clinical trial records.• Support site readiness for regulatory inspections and audits.• Assist in maintaining trial documentation in accordance with regulatory requirements.Required Qualifications• Strong understanding of clinical research processes and clinical trial monitoring• Knowledge of international regulatory guidelines including ICH-GCP• Excellent attention to detail and documentation accuracy• Strong communication and coordination abilities• Ability to manage multiple study sites and monitoring activitiesEducational Requirements:• Bachelor’s degree in Life Sciences• Bachelor’s degree in Pharmacy (B.Pharm)• Degree or certification in Clinical ResearchExperience and Skills:• 0.6 – 2 years of experience in clinical research or CRA roles• Hands-on experience in site monitoring and clinical trial coordination• Strong knowledge of Source Data Verification (SDV) processes• Familiarity with electronic Case Report Forms (eCRF) systems• Good understanding of regulatory documentation and compliance requirements• Ability to coordinate with investigators, sponsors, and clinical teams• Strong documentation review and reporting skills• Willingness to travel for clinical site visitsSalary InsightsFor Clinical Research Associate roles with 0–2 years of experience in India, the typical salary range is between ₹2.4 LPA and ₹4.2 LPA, depending on the candidate’s experience, monitoring exposure, and clinical research expertise.Additional benefits may include professional development programs, clinical research training, travel allowances for monitoring visits, and opportunities for career advancement in the CRO industry.Company OverviewAnaZeal Analyticals and Research Pvt. Ltd. operates in the Clinical Research Organization (CRO) sector, providing clinical trial support, research services, and regulatory compliance expertise. CROs play an essential role in assisting pharmaceutical companies and sponsors in conducting clinical trials efficiently and according to regulatory standards.By working with AnaZeal Analyticals and Research, professionals gain valuable exposure to clinical trial operations, regulatory compliance processes, and real-world monitoring activities. The organization focuses on maintaining high-quality research standards and ensuring that clinical studies are conducted ethically and accurately.FAQs1. What does a Clinical Research Associate do?A Clinical Research Associate monitors clinical trial sites, verifies data accuracy, ensures regulatory compliance, and supports the overall management of clinical trials.2. Is travel required for CRA jobs?Yes, many CRA roles require travel to clinical trial sites for monitoring visits and site management activities.3. What skills are important for a CRA role?Key skills include clinical trial monitoring, regulatory knowledge, documentation review, data verification, and communication with investigators and sponsors.4. What career growth opportunities exist after becoming a CRA?Professionals can advance to Senior CRA, Clinical Trial Manager, Clinical Project Manager, or Regulatory Affairs roles.Application Tips• Highlight your experience with site monitoring and Source Data Verification (SDV).• Mention your knowledge of ICH-GCP guidelines and regulatory compliance.• Include experience related to clinical trial documentation and eCRF systems.• Emphasize your communication skills and ability to coordinate with investigators.• Showcase any clinical research certifications or training programs.• Ensure your resume reflects your willingness to travel and manage site visits.

Why This Role MattersThe biotechnology industry is rapidly evolving, with innovation driving demand for strategic partnerships, market expansion, and commercialization expertise. A Business Development Trainee plays a key role in bridging scientific knowledge with business growth initiatives. This position supports revenue generation, market penetration, and long-term strategic expansion within competitive biotech and pharmaceutical landscapes.For recent biotechnology and pharmaceutical management graduates, this role provides an opportunity to transition from academic knowledge into real-world commercial application. It builds strong foundations in market research, client engagement, strategic planning, and cross-functional collaboration essential skills for long-term success in biotech business careers.Job DescriptionUnique Biotech is hiring Business Development Trainees in Mumbai and Hyderabad. This opportunity is designed for recent graduates (2024, 2025, 2026 pass-outs) who want to combine biotechnology expertise with business strategy and market exposure.The trainee will support business expansion activities, conduct industry research, assist in strategy formulation, and coordinate with internal and external stakeholders. The role requires strong analytical ability, communication skills, and interest in biotech commercialization.Key Features of the Role• Industry exposure Hands-on experience in biotechnology and pharmaceutical markets• Strategy involvement Participation in growth planning and competitive positioning• Client interaction Opportunity to engage in technical and commercial discussions• Market intelligence Experience in industry research and opportunity mapping• Cross-functional learning Collaboration with technical and marketing teams• Career acceleration Clear pathway into Business Development Executive or Manager rolesResponsibilities• Market research Conduct detailed analysis of biotech and pharmaceutical sectors• Strategy support Assist in developing business strategies and growth plans• Client coordination Support technical discussions and client communications• Opportunity identification Identify and evaluate new business opportunities• Proposal development Prepare presentations, proposals, and competitive analysis reports• Team collaboration Coordinate with internal technical and marketing teams• Lead generation Contribute to partnership development and prospect identification• Reporting Maintain structured documentation of market insights and outreach activitiesRequired Qualifications• Academic eligibility M.Tech Biotechnology, B.Tech Biotechnology, MBA/PGDM in Pharmaceutical Marketing Management• Graduation year Recent pass-outs (2024 / 2025 / 2026)• Communication Strong verbal and written communication skills• Analytical skills Ability to interpret market data and identify trends• Business interest Genuine interest in biotech sales, pharma marketing, and business strategy• Professional attitude Willingness to learn and adapt in a corporate environmentEducational Requirements• Bachelor’s or Master’s degree in Biotechnology• MBA/PGDM specialization in Pharmaceutical Marketing Management preferredFreshers seeking entry-level biotech business development jobs in India are strongly encouraged to apply.Experience and Skills• Freshers welcome No prior experience mandatory• Research capability Ability to conduct structured market research• Presentation skills Confidence in preparing professional presentations and reports• Interpersonal ability Comfortable interacting with clients and stakeholders• Commercial awareness Basic understanding of market dynamics and competitive analysis• Organizational skills Ability to manage tasks efficiently and meet deadlinesSalary InsightsEstimated Salary Range: ₹2.8 LPA – ₹4.5 LPA (CTC)Compensation for Business Development Trainee roles in the biotech sector typically falls within this range. Final salary may vary depending on qualifications, interview performance, and company standards.Company OverviewUnique Biotech operates within the biotechnology sector, focusing on innovation-driven solutions and market expansion initiatives. The organization emphasizes growth, strategic partnerships, and the commercialization of biotech expertise.By integrating technical knowledge with business development strategies, Unique Biotech aims to strengthen its presence in competitive pharmaceutical and biotechnology markets. The company promotes professional development, cross-functional collaboration, and exposure to commercial biotech operations.FAQs• Are freshers eligible? Yes, recent pass-outs from 2024, 2025, and 2026 are eligible• Is prior sales experience required? No, but interest in business development is essential• Is this a field sales role? Primarily office-based with potential client interactions• What is the career progression? Growth into Business Development Executive or Manager roles• Are both locations open simultaneously? Positions are available in Mumbai and HyderabadApplication Tips• Highlight technical background Clearly mention biotechnology specialization• Showcase business interest Include projects related to marketing or strategy• Emphasize communication Demonstrate presentation or seminar experience• Add internship details Mention any pharma or biotech industry exposure• Keep resume concise Use structured formatting with measurable achievements• Express career intent Clearly state interest in biotech business development career path

Why This Role MattersCroissance Clinical Research operates within the fast-growing Clinical Research Organization (CRO) sector, supporting pharmaceutical and healthcare companies in drug development and research services. Business Development plays a critical role in expanding partnerships, generating revenue, and strengthening long-term sponsor relationships.This position offers professionals with 1–2 years of experience an opportunity to transition into the strategic side of clinical research. If you are aiming to build a stable and growth-oriented career in the CRO industry, this role provides exposure to sponsor interactions, proposal strategy, and healthcare market expansion.Job DescriptionCroissance Clinical Research is inviting applications for the position of Business Development Executive in Mumbai. The selected candidate will be responsible for identifying business opportunities, developing client relationships, and supporting growth initiatives within the clinical research and pharmaceutical sectors.This role combines strategic communication, market research, and client engagement, making it ideal for candidates with a life sciences or pharmacy background who want to move beyond technical roles into business growth functions.Key Features of the Role• Opportunity to work in the Clinical Research Organization (CRO) sector• Exposure to pharma sponsors and healthcare clients• Direct involvement in proposal preparation and client presentations• Growth-oriented business development career path• Dynamic and collaborative work environment• Long-term career opportunities in clinical research servicesResponsibilities Required• Identifying new business opportunities in clinical research and pharma sectors• Developing and maintaining strong client relationships with sponsors and stakeholders• Supporting proposal preparation, costing discussions, and business presentations• Conducting market research to identify emerging opportunities in life sciences• Coordinating with internal operational teams to ensure seamless service delivery• Representing the organization at industry meetings and networking events• Tracking leads, follow-ups, and maintaining CRM data• Supporting revenue growth targets and business expansion strategiesQualificationsCandidates must possess one of the following qualifications:• Bachelor’s degree in Life Sciences• Bachelor’s degree in Pharmacy• Bachelor’s degree in Biotechnology• Degree in Healthcare or related discipline• Master’s degree in relevant field (preferred)• MBA (Marketing / Healthcare Management) preferred but not mandatoryEducational Requirements• Full-time degree from a recognized university• Strong academic background in healthcare or life sciences• Business or marketing specialization is an added advantageExperience and SkillsExperience• 1–2 years of experience in business development, pharma sales, or clinical research• Experience in CRO environment will be an added advantage• Fresh MBA graduates with internship exposure may also be consideredSkills Required• Strong communication and presentation skills• Client relationship management ability• Basic understanding of clinical trials and pharma industry structure• Market research and competitive analysis skills• Negotiation and persuasion capability• Professional networking skills• Self-motivated and target-driven attitudeSalary InsightsEstimated Salary Range• ₹3.0 LPA – ₹5.0 LPA (based on experience and performance)Additional Benefits:• Career growth opportunities in the clinical research industry• Exposure to pharma sponsors and CRO business models• Performance-based incentives (as per company policy)• Professional networking exposure• Skill development in strategic business functionsCompany OverviewCroissance Clinical Research is a Clinical Research Organization (CRO) providing research and development support services to pharmaceutical, biotechnology, and healthcare companies. CROs play a crucial role in clinical trials, regulatory submissions, and product development support.Working in a CRO environment offers structured exposure to global research standards, sponsor management, and regulatory compliance systems. The company focuses on delivering reliable clinical research services while building strong partnerships within the healthcare ecosystem.FAQsIs prior CRO experience mandatory?No, candidates with pharma sales or business development experience are also eligible.Is MBA compulsory?No, MBA is preferred but not mandatory.What type of career growth can be expected?Progression into Senior Business Development Executive, Business Development Manager, or Strategic Alliances roles.Is this a field-based or office-based role?The role may involve client meetings and networking events along with office coordination.Location of posting?Mumbai.Application Tips• Research basics of clinical research and CRO business models• Understand sponsor-CRO relationships• Prepare examples of client handling or sales achievements• Highlight communication and presentation skills in resume• Be ready to discuss revenue targets or business expansion ideas• Demonstrate knowledge of pharma industry trends

Why This Role MattersThe Pharma (PhD) – Project Management role at SGS India plays a critical role in driving scientific excellence, operational efficiency, and regulatory compliance within pharmaceutical research and testing environments. As pharmaceutical research projects grow increasingly complex, structured project management ensures that timelines, quality standards, and regulatory requirements are consistently met.This position supports the coordination and oversight of pharma research and laboratory testing projects, ensuring smooth execution from initiation to completion. By aligning scientific expertise with project governance, the role directly contributes to delivering reliable, high-quality testing outcomes for clients across the pharmaceutical industry.Working within SGS’s globally recognized quality framework, this role reinforces integrity, sustainability, and operational excellence in laboratory-based pharmaceutical research.Job DescriptionSGS India is seeking a qualified PhD professional for a full-time Project Management role within its pharmaceutical research and testing division. The position is based at the SGS laboratory in Kopar Khairane, Navi Mumbai.The candidate will be responsible for managing pharmaceutical research and laboratory testing projects, ensuring that all deliverables meet scientific, regulatory, and quality standards. The role requires strong coordination skills, an understanding of pharma testing workflows, and the ability to manage timelines, stakeholders, and documentation processes effectively.The selected professional will collaborate with laboratory teams, quality assurance units, and client stakeholders to ensure seamless project execution within a regulated environment.Key Features of the Role• Full-time project management role in pharmaceutical research and testing• Based at SGS laboratory in Kopar Khairane, Navi Mumbai• Exposure to regulated laboratory environments• Coordination of multi-functional scientific teams• Oversight of timelines, budgets, and quality standards• Alignment with global testing and certification benchmarks• Opportunity to work within a globally recognized quality-driven organizationResponsibilities Required• Manage end-to-end pharmaceutical research and testing projects• Develop and monitor project timelines, milestones, and deliverables• Coordinate with laboratory teams to ensure smooth workflow execution• Ensure compliance with regulatory and quality standards• Maintain structured project documentation and reporting• Identify and mitigate operational or technical risks• Facilitate communication between internal teams and external stakeholders• Support quality assurance processes within project lifecycle• Monitor resource allocation and optimize project efficiency• Ensure timely completion of testing assignments as per client requirements• Maintain data integrity and documentation traceability• Contribute to continuous process improvement initiativesQualifications• PhD – Mandatory• Doctorate in Pharmaceutical Sciences or related discipline preferredEducational Requirements• PhD qualification in Pharmaceutical Sciences, Chemistry, Biotechnology, or relevant life sciences discipline• Strong academic background in research methodology and scientific analysisExperience and Skills• Proven project management experience• Experience in pharmaceutical research and testing environments preferred• Understanding of regulated laboratory operations• Knowledge of quality standards and compliance requirements• Strong coordination and leadership skills• Excellent analytical and problem-solving abilities• Strong written and verbal communication skills• Ability to manage multiple projects simultaneously• High attention to detail and documentation accuracy• Risk identification and mitigation capability• Ability to work in cross-functional team environments• Familiarity with laboratory quality systems is an advantageSalary Insights• Competitive salary aligned with industry standards for PhD-level project management roles• Compensation commensurate with experience and expertise• Opportunity for career growth within a globally recognized organizationCompany OverviewSGS India is part of SGS, the world’s leading testing, inspection, and certification company. With 97,000 employees operating across 2,650 offices and laboratories globally, SGS is recognized as the global benchmark for sustainability, quality, and integrity.The organization provides specialized solutions across industries, enabling businesses to become faster, simpler, and more efficient. Within the pharmaceutical domain, SGS delivers high-quality testing and research services aligned with global regulatory and scientific standards.The Navi Mumbai laboratory at Kopar Khairane supports pharmaceutical research and testing operations, ensuring compliance, accuracy, and operational excellence in all service offerings.FAQs• Q: Is a PhD mandatory for this role?A: Yes, a PhD qualification is mandatory.• Q: Is prior pharma testing experience required?A: Experience in pharma research and testing is preferred.• Q: Where is the job location?A: The position is based at SGS laboratory in Kopar Khairane, Navi Mumbai.• Q: Is this a laboratory-based role?A: Yes, the position operates within a laboratory research and testing environment.• Q: Does the role involve client interaction?A: Yes, project management responsibilities may include stakeholder coordination.Application Tips• Highlight project management experience clearly• Emphasize exposure to pharmaceutical research or testing• Demonstrate experience working in regulated laboratory environments• Showcase leadership and coordination skills• Include examples of managing timelines and quality compliance• Mention familiarity with quality systems or certification standards

Why This Role MattersThe Medical Specialist role at Medulla Communications is critical for bridging the gap between scientific accuracy and creative healthcare communication. This position ensures that all medical content is scientifically precise, regulatory-compliant, and creatively compelling. The individual contributes directly to client success by developing materials that effectively communicate complex medical information to diverse target audiences, including healthcare professionals, patients, and internal stakeholders. By combining scientific expertise with creative thinking, the role enhances the agency’s reputation as a global leader in healthcare advertising, ensuring clients’ campaigns are both informative and impactful.Job DescriptionThe Medical Specialist will be responsible for developing and delivering high-quality medical communications for leading pharmaceutical, consumer healthcare, and medical device clients. The role involves understanding clients’ medico-marketing requirements, conducting detailed literature searches, creating scientifically accurate and engaging content, and collaborating with internal and external teams for seamless execution. This role requires a combination of scientific knowledge, creative aptitude, and project management skills to deliver communications across multiple media, including print, digital, video, CME-certified content, and scientific publications.Key Features of the Role• Develop innovative medical content that is both scientifically accurate and creatively engaging.• Collaborate with client servicing, creative, and external teams to deliver integrated healthcare campaigns.• Conduct literature searches and translate scientific insights into clear, compelling communication.• Ensure compliance with regulatory guidelines and scientific accuracy in all communications.• Participate in brainstorming and ideation sessions to provide medical expertise and insights.• Manage multiple projects across media channels, including websites, videos, print collaterals, CME modules, and presentations.• Review content produced by creative teams for accuracy, clarity, and relevance.• Stay updated with clinical, scientific, and industry trends to enhance content quality and innovation.Responsibilities Required• Create and develop medical communications that combine scientific rigor with creative presentation.• Collaborate with internal teams and external vendors to ensure timely and high-quality content delivery.• Conduct extensive literature searches and integrate relevant research findings into communications.• Develop content across multiple media including print, digital, video, scientific publications, CME collaterals, and presentations.• Attend brainstorming and ideation sessions to contribute scientific insights to creative campaigns.• Ensure that all content meets regulatory, legal, and scientific standards.• Manage timelines and prioritize tasks to meet project deadlines.• Mentor and guide junior team members on best practices in scientific writing and medical communication.Qualifications• MBBS – Medicine• Other Graduate – Any Specialization• PG – Any course, any specialization• M.Pharm – Pharmacy• M.Sc – Life Sciences, Biotechnology, Zoology, Botany, Microbiology, or related fieldsEducational Requirements• MBBS, M.Pharm, or M.Sc in Life Sciences or related disciplines.• Postgraduate qualifications in a relevant field are an advantage.Experience and Skills• 2-4 years of experience in medical or scientific writing is preferred.• Strong command of English grammar, composition, and creative writing.• Excellent research skills with the ability to translate complex scientific data into simple, engaging content.• Ability to work collaboratively with internal and external teams.• Flexibility and willingness to learn in a dynamic environment.• Strong project management skills and the ability to handle multiple assignments simultaneously.• Creative thinking, problem-solving, and attention to detail.• Knowledge of medico-marketing, healthcare regulations, and CME content development is an added advantage.Salary Insights• The salary is competitive and commensurate with experience, role responsibilities, and industry standards.• Performance-based incentives may be applicable depending on project outcomes and client satisfaction.Company OverviewMedulla Communications is a global leader in healthcare advertising and communications, recognized for combining scientific rigor with creativity. Since 2015, the agency has won over 20 international awards, including a Grand Prix at Cannes Lions Health, Clio, Global, LIA, and Spikes. Medulla offers end-to-end services, including creative development, advertising, digital solutions, and CME-certified content for pharmaceutical, consumer healthcare, and medical device brands. Its philosophy, “Inhale science, exhale creativity,” emphasizes collaboration among Client Servicing, Medical, and Creative teams to deliver accurate, effective, and innovative healthcare communications globally.FAQs• Q: Is prior medical writing experience mandatory?A: Preferred but not mandatory; strong scientific knowledge and communication skills are essential.• Q: Does this role involve client interaction?A: Yes, occasional client interactions may be required alongside internal collaboration.• Q: Is remote work allowed?A: The role is primarily based in Santacruz, Mumbai, with flexibility depending on project requirements.• Q: What types of media will the content cover?A: Content spans websites, videos, print collaterals, scientific publications, CME modules, and presentations.• Q: Are CME certifications part of the responsibilities?A: Yes, developing CME-certified content may be part of the role.Application Tips• Highlight relevant medical or scientific writing experience in your resume.• Showcase ability to translate complex scientific data into creative and impactful communication.• Demonstrate collaboration and teamwork skills in previous projects.• Include examples of multi-platform content creation if available.• Clearly present your qualifications, experience, and skills.• Emphasize adaptability, continuous learning, and innovative thinking in your application.

Why This Role MattersPharmacovigilance professionals play a critical role in safeguarding public health by monitoring, evaluating, and reporting drug safety data. Aggregate safety reports such as PADERs, PSURs, PBRERs, and Risk Management Plans (RMPs) are essential regulatory documents that ensure ongoing benefit-risk evaluation of medicinal products.As an Officer – Pharmacovigilance at Unichem Laboratories, you will contribute directly to global drug safety compliance, regulatory reporting accuracy, and adherence to international standards such as FDA, ICH-GCP, and GVP guidelines. This role is ideal for pharmacy professionals aiming to build a strong career in drug safety and regulatory science.Job DescriptionUnichem Laboratories is hiring for the position of Officer – Pharmacovigilance (Aggregate Report Drafting) in Mumbai. This is a full-time, permanent opportunity for professionals with 1–6 years of pharmacovigilance experience, particularly in aggregate safety reporting.The selected candidate will be responsible for drafting, reviewing, and maintaining periodic safety reports and ensuring compliance with global regulatory requirements. The role also involves supporting pharmacovigilance operations, conducting training sessions, and collaborating with Medical Affairs and other internal stakeholders.Key Responsibilities• Support execution of pharmacovigilance (PV) activities• Prepare and maintain PV documents, SOPs, and Work Instructions (WIs)• Draft and review aggregate safety reports, including:• Periodic Adverse Drug Experience Reports (PADERs)• Periodic Safety Update Reports (PSURs)• Periodic Benefit-Risk Evaluation Reports (PBRERs)• Risk Management Plans (RMPs)• Ensure compliance with company SOPs and global regulatory requirements• Monitor regulatory authority websites for safety updates and compliance changes• Provide accurate responses to medical information queries• Conduct PV training sessions for internal teams, manufacturing plants, and vendors• Support Medical Affairs in pharmacovigilance-related inquiriesThis position provides comprehensive exposure to global drug safety regulations and aggregate report drafting processes.Eligibility CriteriaEducational Qualification:• B.Pharm (Bachelor of Pharmacy)• M.Pharm (Any Specialization Preferred)Experience:• 1–6 years of pharmacovigilance experience• Hands-on experience in aggregate safety report drafting preferredDesired Skills & Competencies• Strong understanding of international regulatory requirements including FDA, ICH-GCP, and GVP Modules• Knowledge of EU Clinical Trial Directive• Experience in pharmacovigilance aggregate report drafting• Excellent written and verbal communication skills• Strong analytical and decision-making abilities• High attention to detail in drug safety documentation• Ability to work effectively in dynamic, cross-functional teamsSalary & BenefitsCompensation: Competitive salary aligned with industry standards, based on experience and expertise.Additional Benefits:• Opportunity to work with a reputed pharmaceutical organization• Exposure to global regulatory frameworks (FDA, ICH, GVP)• Strong career progression in pharmacovigilance and drug safety• Corporate exposure in a Mumbai-based pharmaceutical setup• Professional development in regulatory documentation and complianceCompany OverviewUnichem Laboratories is a well-established pharmaceutical company engaged in the development, manufacturing, and marketing of pharmaceutical formulations and active pharmaceutical ingredients.The organization emphasizes regulatory compliance, quality standards, and global pharmacovigilance practices. Working at Unichem offers professionals exposure to structured drug safety systems and international reporting standards.FAQsQ: Is aggregate report drafting experience mandatory?Experience in drafting PADERs, PSURs, PBRERs, or RMPs is highly preferred for this role.Q: What level of experience is required?Candidates with 1–6 years of pharmacovigilance experience are eligible to apply.Q: Is this role focused only on documentation?The primary focus is aggregate report drafting, but it also includes PV compliance monitoring, training, and coordination with Medical Affairs.Q: Where is the job location?The position is based in Mumbai.Application Tips• Highlight specific aggregate reports you have drafted or reviewed• Mention exposure to FDA, ICH-GCP, and GVP guidelines• Showcase analytical skills and experience in benefit-risk evaluation• Demonstrate familiarity with SOP-based environments• Prepare to discuss regulatory inspection or audit exposure

Why This Role MattersIn today’s pharmaceutical landscape, scientific accuracy and ethical promotion are critical to maintaining credibility and patient safety. The Medico Marketing function acts as a bridge between medical science and marketing strategy, ensuring that every claim, campaign, and communication is evidence-based and compliant.At Aculife Healthcare Pvt Ltd, part of the reputed Nirma Group, this role offers a strong foundation for Pharm.D graduates to apply their clinical knowledge in a corporate pharmaceutical environment. You will contribute to scientific validation, product positioning, and medical strategy—directly impacting brand integrity and market success.Job DescriptionAculife Healthcare Pvt Ltd is hiring Pharm.D graduates for the position of Medico Marketing Executive at its Mumbai (Malad West) location. This entry-level opportunity is ideal for candidates with strong scientific knowledge, excellent communication skills, and an interest in combining medical expertise with marketing strategy.The selected candidate will support medical and marketing teams by providing evidence-based inputs, validating promotional materials, assisting in product development strategies, and delivering scientific training to internal teams.Key Features of the Role• Entry-level opportunity for Pharm.D graduates (0–1 year experience)• Exposure to pharmaceutical brand strategy and product lifecycle management• Involvement in new product identification and business case preparation• Opportunity to conduct medical training for marketing and field teams• Corporate role in a reputed pharmaceutical organization• Skill development in literature review, content validation, and strategy alignmentResponsibilities• Conduct detailed data mining and literature reviews from credible medical and scientific sources• Provide authoritative, evidence-based medical opinions and responses• Offer scientific inputs for brand strategy execution and new product development• Develop PMS trial protocols, monographs, prescribing information (PI), reference books, visual aids, label (LBL) content, posters, and patient education materials• Validate marketing and promotional content from a medical and regulatory perspective• Identify potential new products and prepare structured business cases• Prepare launch presentations, training manuals, and FAQs for product launch and briefing meetings• Provide scientific rationale for new and existing molecules• Conduct medical training sessions for marketing and field teams• Ensure medical accuracy and compliance in all communication materialsRequired Qualifications• Doctor of Pharmacy (Pharm.D)• 0–1 year of relevant experience (Freshers may apply)• Strong academic foundation in pharmacology, therapeutics, and clinical researchEducational Requirements• Pharm.D (Mandatory)• Additional certifications in clinical research or pharmacovigilance (preferred but not mandatory)Experience and Skills• Strong scientific and clinical knowledge• Excellent communication and interpersonal skills• Proficiency in Microsoft Office (Word, Excel, PowerPoint)• Ability to interpret and analyze clinical literature• Strong presentation and training skills• Attention to detail and regulatory awareness• Analytical thinking and strategic mindset• Ability to work cross-functionally with marketing and product teamsSalary Insights• Competitive entry-level salary as per industry standards• Corporate exposure within a reputed pharmaceutical group• Opportunities for career growth in medical affairs, product management, and strategic marketing• Professional development through hands-on involvement in product launches and brand strategyCompany OverviewAculife Healthcare Pvt Ltd is a pharmaceutical company operating under the umbrella of the Nirma Group, a well-established Indian business group with diversified operations. The company focuses on delivering quality healthcare solutions and maintaining high standards of scientific and regulatory compliance.With a strong emphasis on innovation and ethical practices, Aculife Healthcare provides an environment where medical knowledge and business strategy intersect, making it an excellent platform for Pharm.D graduates seeking corporate pharmaceutical careers.FAQsQ: Are freshers eligible for this role?Yes, candidates with 0–1 year of experience are eligible to apply.Q: Is this a field-based role?No, this is primarily a corporate office-based role in Mumbai (Malad West).Q: What growth opportunities are available?Career progression into Medical Affairs, Product Management, or Strategic Marketing roles is possible based on performance.Q: Is prior marketing experience required?No prior marketing experience is mandatory; strong scientific knowledge is essential.Application Tips• Highlight your Pharm.D qualification prominently• Mention any academic projects, internships, or clinical case work• Showcase literature review or research experience• Emphasize presentation and communication skills• Demonstrate interest in pharmaceutical marketing and product strategy

Why This Role MattersAccurate medical documentation is the backbone of healthcare, insurance processing, and legal review systems. Behind every well-prepared case summary is a professional who understands medical terminology, clinical context, and documentation structure.As a Medical Record Summarizer, you play a crucial role in transforming complex, unstructured medical documents into clear, concise, and structured summaries. Your analytical skills directly impact the quality of decisions made by healthcare providers, legal professionals, and insurance teams.For B.Pharm freshers, this is an excellent opportunity to enter the healthcare documentation and medical review domain while building strong analytical and domain-specific skills.Job DescriptionWe are seeking detail-oriented and analytical B.Pharm graduates (Freshers) for the role of Medical Record Summarizer. The selected candidate will be responsible for reviewing raw medical records provided by clients, identifying relevant clinical information, and preparing structured summaries as per defined guidelines.This role requires strong comprehension skills, good English proficiency, attention to detail, and the ability to extract essential data accurately from large volumes of medical documentation.Key Features of the Role• Entry-level opportunity for B.Pharm graduates• Exposure to real-world medical documentation and case analysis• Skill development in medical summarization and documentation review• Structured training and process-based work environment• Professional growth in healthcare documentation domain• Office-based role with standard working hoursResponsibilities• Analyze and review raw medical documents provided by clients• Identify and list relevant medical records systematically• Cherry-pick and prepare essential clinical information• Summarize medical records in a clear, structured format• Ensure quality and accuracy as per client guidelines• Maintain consistency in documentation standards• Follow data confidentiality and compliance protocols• Meet daily productivity and quality targets• Coordinate with quality control teams for feedback and improvementsRequired Qualifications• Bachelor of Pharmacy (B.Pharm)• Freshers are eligible to apply• Basic understanding of medical terminology preferredEducational Requirements• B.Pharm (Mandatory)• Strong foundation in pharmacology, pathology, and basic clinical conceptsExperience and Skills• Excellent comprehension and analytical skills• Strong knowledge of English (grammar, punctuation, sentence structure)• Ability to read and understand medical documents effectively• Capability to extract and summarize essential clinical data• Sound knowledge of Microsoft Word and Excel• Typing speed of approximately 30–40 words per minute• Good internet research and searching skills• High attention to detail and accuracy• Ability to work with structured guidelines and deadlines• Knowledge of medical terminology (preferred but not mandatory)Salary Insights• Competitive entry-level salary• Opportunity to gain domain expertise in medical documentation• Skill-based growth and internal advancement opportunities• Structured learning environment for fresh graduatesCompany OverviewThe hiring organization operates in the healthcare documentation and medical records management domain, supporting clients with accurate and structured medical summaries. The company emphasizes quality, confidentiality, and compliance while offering fresh graduates a platform to build foundational expertise in medical data analysis.With a focus on training and process-driven excellence, the organization provides an environment where analytical skills and attention to detail are valued and rewarded.FAQsQ: Are freshers eligible?Yes, B.Pharm freshers are encouraged to apply.Q: Is prior experience in medical summarization required?No prior experience is required; training will be provided.Q: Is medical terminology knowledge mandatory?It is preferred but not mandatory.Q: What software skills are required?Basic proficiency in Microsoft Word and Excel is required.Application Tips• Highlight your B.Pharm qualification clearly• Emphasize analytical and comprehension strengths• Mention typing speed if it meets the requirement• Showcase academic exposure to pharmacology and clinical subjects• Demonstrate attention to detail in your resume formatting

Why This Role MattersPharmacovigilance Agreements (PVAs) are critical legal and operational documents that define safety responsibilities between marketing authorization holders and partners. A well-drafted and compliant PVA ensures clear accountability, regulatory compliance, and seamless safety data exchange across global stakeholders.At Tata Consultancy Services (TCS), this role supports global clients within Business Process Services by drafting, reviewing, and managing PVAs in alignment with international pharmacovigilance regulations and company standards.Job DescriptionTCS is hiring experienced Pharmacovigilance professionals for the role of Executive / Senior Executive – Pharmacovigilance Agreements Specialist in Mumbai.The position focuses on drafting, reviewing, maintaining, and monitoring Global and Local Pharmacovigilance Agreements while ensuring compliance with ICH guidelines and Good Pharmacovigilance Practices (GVP).Key Features of the Role• Draft and review Global and Local Pharmacovigilance Agreements (PVAs)• Ensure compliance with ICH and global GVP regulations• Manage PVA trackers, repositories, and reconciliation activities• Monitor compliance of effective PVAs and prepare dashboards• Coordinate with cross-functional and client stakeholders• Manage PVA mailbox and communication workflows• Support project documentation and operational updatesResponsibilities• Draft new PVAs and revise existing agreements as per company standards• Review PVAs for quality, completeness, and regulatory alignment• Address internal and collaborating company comments on agreements• Manage dedicated PVA mailbox and ensure timely communication• Announce new or revised PVAs to relevant stakeholders• Maintain and update global PVA trackers including reconciliation activities• Perform compliance monitoring of active PVAs and prepare dashboards• Upload and maintain PVA documentation in company repository systems• Assist Project Manager or designee in updating project trackers and documentation• Attend team meetings and provide updates on PVA status and operational issuesRequired Qualifications• 3–7 years of experience in Pharmacovigilance• Strong knowledge of global pharmacovigilance regulations (ICH, GVP Modules)• Hands-on expertise in drafting and managing Global and Local PV Agreements• Experience handling contractual pharmacovigilance arrangementsEducational Requirements• Bachelor of Pharmacy (B.Pharm)• Master of Pharmacy (M.Pharm)• Bachelor of Science (B.Sc)• Master of Science (M.Sc)Experience and Skills• Strong understanding of contractual PV obligations• Experience managing PVA trackers and compliance dashboards• Knowledge of global regulatory frameworks and safety exchange processes• Excellent documentation, communication, and stakeholder coordination skills• Proficiency in MS Office tools• Ability to manage multiple agreements and timelines simultaneouslySalary Insights• Competitive compensation aligned with experience• Opportunity to work with global pharmaceutical clients• Exposure to international contractual pharmacovigilance frameworksFAQsQ: Is prior PVA drafting experience mandatory?Yes, hands-on experience with Global and Local PV Agreements is required.Q: Does the role involve client interaction?Yes, coordination with collaborating companies and internal stakeholders is part of the role.Q: Is regulatory knowledge important?Strong understanding of ICH and GVP modules is essential.Application Tips• Clearly mention PVA drafting and review experience• Highlight exposure to global pharmacovigilance regulations• Include examples of compliance monitoring or dashboard preparation• Emphasize stakeholder coordination and documentation management skills

Why This Role MattersPharmacovigilance (PV) training is critical to ensure that all employees, subsidiaries, partners, and vendors are aware of global safety standards, regulatory requirements, and internal processes. Well-trained personnel reduce compliance risks, improve safety data quality, and support overall regulatory adherence.In this role at Fidelity Health Services, you will manage global PV and non-PV training programs, track compliance, and contribute to the development of departmental processes and training methodologies. This position directly impacts the competency and readiness of teams operating across multiple geographies.Job DescriptionFidelity Health Services is hiring an Executive / Senior Executive to lead and manage pharmacovigilance training initiatives. Based in Navi Mumbai, this role involves planning, executing, and monitoring PV and non-PV training activities for employees, subsidiaries, partners, and vendors globally.The role requires coordination with internal teams, e-learning platforms, and global stakeholders to ensure compliance with regulatory training requirements. You will also maintain training records, update documentation, and contribute to process improvements.Key Features of the Role• Manage global PV and non-PV training programs• Oversee e-learning systems and portals for effective training delivery• Track training compliance and generate reports for management• Maintain accurate training documentation and records• Contribute to SOP, Work Instructions (WI), and Working Practice System (WPS) updates• Support departmental process improvements and methodology development• Perform impact analysis for PV training compliance strategiesResponsibilities• Plan and manage pharmacovigilance and non-pharmacovigilance training programs globally• Administer and maintain e-learning platforms and portals• Track employee and partner compliance with mandatory training• Conduct cyclical review and updates of training-related documentation• Manage documentation for all training activities, including records and reports• Assist in developing departmental processes, procedures, and best practices• Provide inputs into SOPs, WIs, WPS, and other relevant procedural documents• Perform impact analysis of training compliance and recommend improvementsRequired Qualifications• 2–4 years of experience in training management within a pharmaceutical or healthcare environment• Experience in pharmacovigilance training is preferred but not mandatory• Familiarity with e-learning platforms and compliance tracking systems• Strong documentation and organizational skillsEducational Requirements• Bachelor of Pharmacy (B.Pharm)• Master of Pharmacy (M.Pharm)• Bachelor of Ayurvedic Medicine & Surgery (BAMS)• Bachelor of Homeopathic Medicine & Surgery (BHMS)Experience and Skills• Ability to plan and deliver training programs across multiple regions• Knowledge of pharmacovigilance processes and compliance requirements• Excellent communication and interpersonal skills• Strong analytical and organizational skills• Experience managing global stakeholders and training portalsSalary Insights• Competitive salary based on experience and qualification• Career growth within PV and global training management• Exposure to multinational operations and regulatory training complianceCompany OverviewFidelity Health Services is a global provider of pharmacovigilance and regulatory compliance services. The organization supports multinational pharmaceutical companies with PV operations, training, aggregate reporting, and safety compliance. Fidelity Health Services emphasizes process excellence, global regulatory adherence, and continuous development of personnel.FAQsQ: Is prior PV experience mandatory?Experience in PV is preferred but candidates with general pharmaceutical training experience will also be considered.Q: Does the role involve global stakeholders?Yes, the role manages training for employees, subsidiaries, partners, and vendors worldwide.Q: Are e-learning systems used?Yes, the candidate will manage and maintain e-learning platforms and compliance portals.Application Tips• Highlight experience in training coordination and compliance tracking• Include exposure to e-learning management systems• Showcase ability to manage documentation and updates for SOPs, WIs, and WPS• Demonstrate familiarity with PV or regulatory training processes

Why This Role MattersDrug Safety Specialists play a crucial role in ensuring accurate reconciliation, regulatory compliance, and effective exchange of global safety information. Strong reconciliation and compliance monitoring processes protect patient safety and maintain regulatory trust.At Fidelity Health Services, this role supports global pharmacovigilance operations by managing safety reconciliation activities, reference safety information updates, and regulatory database reviews.Job DescriptionFidelity Health Services is hiring an Executive / Senior Executive – Drug Safety Specialist for its Navi Mumbai location. The role focuses on safety reconciliation, compliance monitoring, global safety information exchange, and regulatory data review.The selected candidate will coordinate with internal PV teams and global stakeholders to ensure accurate reconciliation of safety data and timely documentation updates.Key Features of the Role• Exposure to global pharmacovigilance operations• Hands-on experience in safety reconciliation and compliance monitoring• Interaction with regulatory safety databases• Involvement in global product lifecycle safety management• Opportunity to grow within drug safety operationsResponsibilities• Manage safety reconciliation and compliance monitoring activities for clients• Perform reconciliation of Reference Safety Information (RSI) for client products• Conduct data mining and review of FDA’s Adverse Event Reporting System (FAERS) and other regulatory databases• Edit, review, and reconcile Consolidated Global Product Lists• Manage global exchange of safety information for product approvals, launches, cancellations, and RSI updates• Maintain and update documentation related to safety reconciliation• Coordinate with cross-functional teams for issue resolution• Ensure regulatory compliance and audit readinessRequired Qualifications• 5–8 years of experience in the Pharmacovigilance domain• Strong experience in safety reconciliation and compliance monitoring• Proficiency in MS Excel• Experience in mailbox management and safety communication trackingEducational Requirements• Bachelor of Pharmacy (B.Pharm)• Master of Pharmacy (M.Pharm)Experience and Skills• Strong understanding of pharmacovigilance processes• Experience with global safety information exchange workflows• Knowledge of FAERS and regulatory safety databases• Analytical and detail-oriented approach• Good documentation and coordination skills• Ability to manage multiple client deliverables and timelinesSalary Insights• Competitive compensation based on experience• Exposure to global drug safety projects• Career progression opportunities in reconciliation and complianceCompany OverviewFidelity Health Services provides end-to-end pharmacovigilance and regulatory services to global pharmaceutical companies. The organization specializes in safety reconciliation, aggregate reporting, compliance monitoring, and regulatory documentation support.FAQsQ: Is prior reconciliation experience mandatory?Yes, hands-on experience in safety reconciliation is required.Q: Does the role involve regulatory database review?Yes, including FAERS and other global safety databases.Q: Is this a client-facing role?The role involves coordination with clients and internal PV teams.Application Tips• Highlight reconciliation experience clearly• Mention exposure to FAERS or regulatory databases• Showcase Excel proficiency (pivot tables, tracking sheets)• Include examples of compliance monitoring or audit support experience

Why This Role MattersSafety Writers are essential to maintaining the integrity, accuracy, and regulatory compliance of aggregate safety reports. Monitoring documentation flow, tracking submissions, and ensuring timely closure of action items directly impact regulatory trust and patient safety.At Fidelity Health Services, this role supports structured aggregate reporting processes and compliance monitoring for global pharmacovigilance operations.Job DescriptionFidelity Health Services is hiring an Executive Safety Writer / Senior Executive for its Navi Mumbai location. The role focuses on supporting aggregate report management, document tracking, compliance monitoring, and assisting in analysis of nonconformance-related action items.The selected candidate will work closely with medical writers, aggregate reporting teams, and quality stakeholders to ensure documentation accuracy and timely workflow management.Key Features of the Role• Exposure to global aggregate reporting workflows• Involvement in report tracking and compliance monitoring• Coordination with medical writing and PV teams• Opportunity to strengthen quality oversight skills• Career growth within pharmacovigilance operationsResponsibilities• Verify arrival of source documents and final signed aggregate reports• Monitor and update online aggregate report trackers• Ensure documentation completeness and version control• Track submission timelines and report status updates• Assist in analysis and follow-up of nonconformance action items• Coordinate with internal stakeholders for document reconciliation• Maintain compliance records and audit readiness documentation• Support safety writing and reporting teams as required• Identify process gaps and escalate issues appropriatelyRequired Qualifications• 2–4 years of experience in safety writing and aggregate reporting• Familiarity with aggregate report workflows (PSUR, PBRER, PADER, etc.)• Experience in documentation tracking and compliance monitoringEducational Requirements• B.Pharm• M.Pharm• BHMS• BAMSExperience and Skills• Strong understanding of aggregate reporting processes• Experience in documentation control and tracker management• Basic knowledge of pharmacovigilance regulations• Good analytical and coordination skills• Proficiency in MS Office (especially Excel)• Attention to detail and compliance-focused approach• Ability to manage timelines and multiple tasksSalary Insights• Competitive compensation aligned with experience• Exposure to global PV and aggregate reporting operations• Career advancement opportunities in safety writing and complianceCompany OverviewFidelity Health Services provides end-to-end pharmacovigilance and regulatory services to global pharmaceutical clients. The organization specializes in aggregate reporting, safety reconciliation, compliance monitoring, and structured PV documentation support.FAQsQ: Is hands-on aggregate report drafting required?Experience in safety writing and aggregate reporting processes is required.Q: Does the role involve compliance monitoring?Yes, tracking documentation and nonconformance action items is a key responsibility.Q: Is this a client-facing role?Primarily internal coordination, but interaction with cross-functional teams is involved.Application Tips• Mention types of aggregate reports handled• Highlight experience with report trackers and documentation systems• Include exposure to quality audits or nonconformance management• Emphasize organizational and compliance skills

Why This Role MattersSafety Medical Writers play a crucial role in evaluating and communicating the benefit–risk profile of medicinal products through structured regulatory documents. Aggregate reports such as PSUR, PBRER, PADER, and RMP are essential for maintaining product approvals and ensuring ongoing patient safety in global markets.At Fidelity Health Services, the Safety Medical Writer contributes to high-quality aggregate report preparation, regulatory compliance, and client-focused pharmacovigilance operations.Job DescriptionFidelity Health Services is hiring a Safety Medical Writer for its Mumbai location. The role focuses on drafting, reviewing, and managing Aggregate Reports (ARs) including PSUR, PBRER, PADER, RMP, and Annual Safety Reports.The selected candidate will collaborate with ICSR teams, regulatory stakeholders, and global clients to ensure accurate data compilation, medical evaluation, and timely regulatory submissions.Key Features of the Role• Hands-on experience in aggregate safety report writing• Exposure to global regulatory reporting requirements• Direct coordination with clients and cross-functional PV teams• Involvement in submission planning and strategy• Growth opportunity in medical writing and risk managementResponsibilities• Draft and quality review PSUR, PBRER, PADER, RMP, and Annual Safety Reports• Develop submission strategies and ensure adherence to timelines• Conduct kick-off meetings with clients and internal stakeholders• Generate line listings and summary tabulations from processed ICSRs• Review XML data extracted from global safety databases• Identify safety signals and data inconsistencies• Ensure compliance with global regulatory guidelines• Maintain documentation for audit readiness• Resolve issues related to aggregate report preparation• Support additional pharmacovigilance and medical writing activitiesRequired Qualifications• 2–3 years of experience in aggregate safety report drafting and review• Strong knowledge of global PV regulatory frameworks• Experience handling PADER, PSUR, PBRER, and RMP documentationEducational Requirements• M.Pharm• B.Pharm• BAMS• BHMS• BDS Experience and Skills• Strong medical writing and analytical skills• Knowledge of ICSR processing and safety databases• Experience in line listing and tabulation generation• Familiarity with XML data extraction• Good understanding of benefit-risk evaluation concepts• Strong communication and stakeholder coordination skills• Detail-oriented with strong compliance focusSalary Insights• Competitive compensation based on experience and expertise• Exposure to global regulatory markets• Career progression in medical writing and risk managementCompany OverviewFidelity Health Services is a pharmacovigilance and regulatory services organization offering comprehensive drug safety solutions to global pharmaceutical clients. The company specializes in aggregate reporting, reconciliation management, compliance monitoring, and regulatory documentation.FAQsQ: Is aggregate reporting experience mandatory?Yes, hands-on experience in drafting PSUR/PBRER/PADER/RMP is required.Q: Does the role involve client interaction?Yes, coordination with clients and internal stakeholders is part of the role.Q: Is healthcare professional qualification acceptable?Yes, candidates with BAMS, BHMS, BDS, B.Pharm, or M.Pharm qualifications are eligible.Application Tips• Highlight number and type of aggregate reports handled• Mention global markets supported (US, EU, ROW)• Include safety database experience• Showcase medical writing and regulatory compliance expertise

Why This Role MattersPharmacovigilance reconciliation and compliance monitoring are critical to maintaining global drug safety standards. Accurate reconciliation of safety data ensures consistency between regulatory submissions, reference safety information (RSI), and global product databases—ultimately safeguarding patient health and maintaining regulatory compliance.At Fidelity Health Services, this role plays a key part in managing global safety information exchange, reconciliation activities, and compliance oversight for multiple clients.Job DescriptionFidelity Health Services is seeking experienced Pharmacovigilance professionals for its Navi Mumbai location. The position focuses on safety reconciliation, compliance monitoring, RSI management, and global exchange of safety information across product lifecycles.The selected candidate will support client-specific safety operations, manage global product listings, and ensure regulatory alignment with international pharmacovigilance requirements.Key Features of the Role• Exposure to global pharmacovigilance operations• Involvement in safety reconciliation and compliance monitoring• Interaction with international regulatory databases (e.g., FAERS)• Management of global safety information exchange• Opportunity to work with multinational client portfoliosResponsibilities• Manage safety reconciliation activities for assigned clients• Perform reconciliation of Reference Safety Information (RSI)• Conduct data mining and review of FDA’s FAERS and other regulatory databases• Edit, review, and reconcile Consolidated Global Product Lists• Manage global exchange of safety information related to product approvals, launches, cancellations, and RSI updates• Monitor compliance metrics and reporting timelines• Maintain and update safety reconciliation documentation• Ensure data accuracy and regulatory compliance• Coordinate with cross-functional PV and regulatory teams• Support audit readiness and documentation reviewsRequired Qualifications• 5–8 years of experience in Pharmacovigilance domain• Hands-on experience in safety reconciliation and compliance monitoring• Experience working with global regulatory databases• Proficiency in MS Excel and mailbox managementEducational Requirements• Bachelor of Pharmacy• Master of PharmacyExperience and Skills• Strong understanding of global PV regulations• Experience in RSI reconciliation and safety database review• Knowledge of FAERS and regulatory data mining• Good analytical and documentation skills• Strong attention to detail and compliance mindset• Ability to manage multiple client deliverables• Effective communication and coordination skillsSalary Insights• Competitive compensation based on PV experience• Exposure to global pharmacovigilance operations• Growth opportunities in safety compliance and regulatory functionsCompany OverviewFidelity Health Services is a pharmacovigilance and regulatory support organization providing end-to-end drug safety services to global pharmaceutical clients. The company specializes in safety operations, reconciliation management, and compliance monitoring in regulated markets.FAQsQ: Is reconciliation experience mandatory?Yes, hands-on experience in safety reconciliation is required.Q: Is FAERS knowledge important?Yes, data mining and review of FAERS and regulatory databases is a key responsibility.Q: Does the role involve global coordination?Yes, management of global safety information exchange is part of the role.Application Tips• Highlight reconciliation projects handled• Mention RSI management experience• Include exposure to FAERS or regulatory databases• Emphasize Excel proficiency and compliance monitoring expertise

Why This Role MattersThe Medical Writing Associate ensures accurate, clear, and regulatory-compliant documentation of medical and scientific content. By preparing medical summaries and supporting documentation, the role contributes to clinical research, regulatory submissions, and scientific communication. This position ensures that pharmaceutical and life sciences data are communicated effectively, supporting patient safety, regulatory compliance, and informed decision-making.Job DescriptionThe Medical Writing Associate is responsible for preparing and editing medical summaries, understanding and applying medical terminology, and following regulatory standards. The role requires strong writing skills, attention to detail, and proficiency in data collection and analysis. Candidates will undergo training and evaluation through tests of medical terms, grammar, typing, and medical summary writing to ensure readiness for the role.Key Features Of The Role• Prepare and edit medical summaries and related documentation• Apply knowledge of medical terms and regulatory standards in documentation• Collect, analyze, and interpret data accurately• Ensure accuracy, clarity, and attention to detail in all written outputs• Follow internal guidelines, SOPs, and regulatory compliance standards• Work collaboratively with team members and supervisors to ensure high-quality outputs• Participate in tests and training to demonstrate proficiency in medical writing skillsResponsibilities• Write and edit medical summaries based on clinical and scientific data• Maintain accuracy and consistency in terminology and documentation• Collect and analyze relevant data to support writing tasks• Follow regulatory standards and internal quality guidelines• Demonstrate strong attention to detail and ensure high-quality output• Participate in pre-interview tests including medical terms, grammar, typing, and summary writing• Complete training program to gain proficiency in company processes and medical writing standards• Communicate effectively with team members and managementRequired QualificationsEducational Requirements• Bachelor's degree in Pharmacy • B.Sc in Life SciencesExperience And Skills• Strong command of English grammar and writing skills• Familiarity with medical terminology and scientific concepts• Typing speed of 20–25 WPM or higher with ≥95% accuracy• Knowledge of relevant regulatory standards and documentation processes• Good communication skills, both verbal and written• Data collection, analysis, and attention to detailSalary Insights• Stipend provided during 1-month training period• Day shift (9:00 AM to 6:00 PM) with 1 working Saturday• Compensation after training as per industry standards and company normsCompany OverviewVitality Business Support Services provides specialized support services to the pharmaceutical and life sciences industries. The company emphasizes training, skill development, and quality documentation, ensuring employees are well-prepared to deliver high-quality medical writing outputs.FAQsQ: What tests will I undergo before the interview?A: Medical Terms MCQ (20), Medical Summary Writing Test, Basic Grammar Test (20 MCQ), and Typing Test.Q: Is training provided?A: Yes, a 1-month training program with stipend is provided.Q: What qualifications are required?A: B.Pharm or B.Sc in Life Sciences with strong writing and typing skills.Application Tips• Highlight your medical or life science education and writing experience• Showcase proficiency in medical terms, grammar, and typing accuracy• Emphasize attention to detail and analytical skills• Prepare for pre-interview tests to demonstrate readiness for the role

Why This Role MattersThe Regulatory Affairs Associate plays a key role in preparing, reviewing, and managing regulatory dossiers to ensure compliance with global regulations. By handling CTD dossiers, process and analytical method validations, and responding to queries from regulatory authorities, this role supports timely product approvals and contributes to the overall success of the organization. The position ensures high-quality submissions, regulatory compliance, and smooth communication with authorities, enabling Apex Drug House to bring safe and effective products to market.Job DescriptionThe Regulatory Affairs Associate is responsible for preparing and reviewing regulatory dossiers, managing process validation and analytical method validation documents, and addressing queries from regulatory bodies. The role requires close collaboration with cross-functional teams, attention to detail, and thorough knowledge of regulatory requirements to ensure accurate and timely submissions. The position supports both local and international regulatory submissions, contributing to Apex Drug House’s mission of delivering high-quality pharmaceutical products.Key Features Of The Role• Prepare and review CTD dossiers for regulatory submissions• Review and evaluate process validation and analytical method validation documents• Handle queries and responses from different regulatory authorities• Ensure submissions comply with applicable regulations and agency guidelines• Maintain up-to-date knowledge of regulatory requirements and industry standards• Collaborate with cross-functional teams including Quality, Production, and R&D• Support preparation of responses to deficiencies or additional information requests• Maintain accurate records of all regulatory submissions and correspondenceResponsibilities• Draft, compile, and review regulatory dossiers, ensuring accuracy and completeness• Evaluate process validation and analytical method validation documentation• Respond to queries from local and international regulatory authorities• Ensure compliance with internal SOPs and global regulatory guidelines• Support cross-functional teams with regulatory guidance during product development• Track submission status and maintain regulatory documentation archives• Assist in audits and regulatory inspections, providing relevant dossiers and supporting documentation• Monitor updates to regulations and implement changes to ensure compliance• Contribute to continuous improvement of regulatory processes and documentation standardsRequired QualificationsEducational Requirements• Graduate or Postgraduate degree (B. Pharma / M. Pharma preferred)Experience And Skills• 3–7 years of experience in a regulatory affairs or similar profile• Experience in preparation and review of CTD dossiers• Knowledge of process validation and analytical method validation requirements• Experience in handling regulatory queries from authorities• Strong attention to detail, organizational, and documentation skills• Good communication and interpersonal skills• Ability to collaborate with cross-functional teams and meet submission timelinesSalary Insights• Compensation as per company norms and industry standards• Opportunities for career growth and professional development• Exposure to regulatory submissions and interactions with local and international authoritiesCompany OverviewApex Drug House is a pharmaceutical company committed to delivering high-quality medicines globally. The company focuses on regulatory compliance, innovation, and scientific rigor to ensure safe and effective products. Apex Drug House fosters a collaborative culture, providing employees opportunities to contribute to drug development and regulatory success.FAQsQ: What type of regulatory documents will I handle?A: CTD dossiers, process validation reports, analytical method validation documents, and responses to regulatory queries.Q: Will I interact with regulatory authorities?A: Yes, the role involves addressing queries and communications with local and international authorities.Q: Is prior regulatory experience required?A: Yes, 3–7 years of experience in a regulatory affairs or similar role is required.Application Tips• Highlight experience in CTD dossier preparation and review• Emphasize knowledge of process validation and analytical method validation• Showcase experience handling regulatory queries• Demonstrate strong attention to detail and ability to manage timelines• Include examples of successful submissions or approvals

Why This Role MattersIn today’s evidence-driven healthcare environment, scientific credibility and ethical engagement are essential to building trust with healthcare professionals. Medical Affairs serves as the bridge between clinical research and real-world practice, ensuring that accurate, balanced, and non-promotional scientific information reaches key stakeholders.This role plays a critical part in strengthening therapy-area expertise, supporting evidence-based discussions, and aligning product strategies with clinical insights. By maintaining compliance while delivering high-quality scientific engagement, the Medical Affairs Executive helps enhance patient outcomes and reinforce the organization’s reputation for medical integrity.Job DescriptionWe are seeking a highly driven Medical Affairs professional to provide scientific and clinical expertise across assigned therapy areas. This field-based role focuses on delivering non-promotional medical support, engaging key external stakeholders, and partnering cross-functionally to strengthen product strategy and customer relationships.The position requires deep therapy-area knowledge, strong communication skills, and the ability to translate complex clinical data into meaningful scientific discussions. The candidate will work closely with Sales, Marketing, and R&D teams while maintaining a strict distinction between promotional and non-promotional activities.This is predominantly a field-based role, requiring approximately 90% travel for scientific engagement and stakeholder interactions.Key Features of the Role• Field-based scientific engagement role• Non-promotional medical communication focus• Direct interaction with Key Opinion Leaders (KOLs)• Involvement in advisory boards, CMEs, and medical events• Cross-functional collaboration with commercial and R&D teams• Contribution to medical strategy developmentResponsibilities• Interpret and communicate clinical data, research findings, and therapy-area updates to internal and external stakeholders• Maintain in-depth knowledge of company products and competitor products• Evaluate scientific literature and assess study methodologies• Provide balanced medical and scientific support to healthcare professionals• Conduct scientific discussions based on published literature and clinical evidence• Support advisory boards, CMEs, conferences, and other medical meetings• Respond to unsolicited medical queries in compliance with regulatory guidelines• Collect and share field insights with Marketing, Sales, and R&D teams• Maintain clear separation between promotional and non-promotional engagements• Ensure all activities comply with regulatory and company policies• Maintain accurate documentation of KOL interactions and scientific discussions• Provide scientific training and product knowledge support to internal teams• Contribute to development and execution of medical strategies aligned with business objectives• Support continuous improvement initiatives within Medical AffairsRequired Qualifications• Strong understanding of clinical research principles• Therapy-area expertise with scientific depth• Ability to interpret and present complex clinical data• Knowledge of ethical guidelines governing medical engagement• Strong stakeholder management capabilitiesEducational Requirements• BDS / B.Pharm / M.Pharm / Pharm.DCandidates with a strong academic foundation and demonstrated interest in Medical Affairs are encouraged to apply.Experience and Skills• Relevant experience in Medical Affairs, Clinical Research, or Scientific Engagement preferred• Strong knowledge of therapeutic areas and evidence-based medicine• Excellent communication and presentation skills• Ability to build professional relationships with healthcare professionals• High level of scientific curiosity and analytical thinking• Ethical and compliance-oriented approach• Strong interpersonal skills• Ability to manage extensive travel (90% field-based role)• Capability to work independently while collaborating cross-functionallySalary InsightsCompensation is aligned with industry standards for field-based Medical Affairs professionals. Salary may vary based on therapeutic expertise, geographic coverage, and prior experience in scientific engagement roles.Additional benefits may include travel allowances, performance incentives, and health coverage as per company policy.Company OverviewThe organization operates within the pharmaceutical/healthcare sector and focuses on strengthening scientific partnerships with healthcare professionals. Through ethical engagement, evidence-based discussions, and strong therapy-area expertise, the company aims to improve clinical understanding and support optimal patient care.The culture emphasizes scientific excellence, compliance integrity, collaboration, and continuous professional development.FAQsIs this a promotional sales role?No, this is a non-promotional Medical Affairs role focused on scientific engagement.Does this role require field travel?Yes, approximately 90% of the role is field-based.Is prior Medical Affairs experience mandatory?Experience in Medical Affairs or clinical research is preferred but strong therapy-area knowledge is essential.Will the role involve interaction with KOLs?Yes, engaging with Key Opinion Leaders and healthcare professionals is a core responsibility.Is compliance training required?Yes, all activities must align with regulatory and company compliance standards.Application Tips• Highlight therapy-area expertise and clinical knowledge• Mention experience conducting scientific discussions or CMEs• Showcase literature evaluation and data interpretation skills• Demonstrate stakeholder engagement experience• Emphasize compliance awareness and ethical conduct• Quantify field engagement or KOL interaction experience if possible

Why This Role MattersIn today’s evolving food industry, regulatory compliance and supplier quality assurance are essential to ensure product safety, brand protection, and global market access. With increasing regulatory scrutiny across the India, Middle East, and Africa (IMEA) region, organizations must maintain strong oversight of raw material approvals, certifications, and supplier documentation.This role ensures that every ingredient and packaging material meets regional and international regulatory standards. By strengthening supplier compliance systems and collaborating cross-functionally, the position directly supports consumer safety, sustainability commitments, and operational excellence.Job DescriptionThe Senior Supplier Quality & Regulatory Compliance Manager – IMEA is responsible for managing supplier documentation, regulatory compliance, and raw material risk assessment across the region. The role works closely with Procurement, R&D, Quality, and global compliance teams to ensure materials meet food safety standards and regulatory requirements.The position focuses on supplier assurance, audit readiness, certification tracking, and documentation accuracy while driving continuous improvement initiatives.Key Features of the Role• Regional responsibility for supplier compliance across IMEA• Cross-functional coordination with R&D and Procurement• Oversight of supplier certifications and documentation systems• Risk assessment and mitigation planning• Audit preparation and sustainability documentation support• Exposure to global regulatory standardsResponsibilities• Manage supplier documentation including specifications, certifications, and compliance declarations• Ensure raw materials and packaging meet regulatory and food safety requirements• Support onboarding and approval of new suppliers and materials• Conduct supplier risk assessments and ensure corrective actions• Track certification validity and maintain updated compliance records• Communicate with suppliers to obtain regulatory and sustainability data• Support customer documentation requirements• Assist in internal and external audits• Monitor regulatory updates affecting raw materials• Ensure compliance with import and export requirements• Drive improvements in supplier quality systemsRequired Qualifications• Strong understanding of food regulatory compliance and supplier assurance• Knowledge of risk assessment frameworks• Familiarity with ISO standards such as ISO 9000 and ISO 14000• Ability to manage documentation across multiple geographies• Strong analytical and coordination skillsEducational Requirements• MSc in Food Science, Chemistry, Biotechnology, Biochemistry, Regulatory Affairs, or NutritionEquivalent scientific qualifications may also be considered.Experience and Skills• Minimum 8+ years of experience in supplier quality or regulatory compliance• Experience handling global customer and regulatory documentation• Familiarity with digital documentation management systems• Knowledge of IMEA regulatory frameworks• Experience supporting sustainability and compliance initiatives• Strong communication and stakeholder management skills• Problem-solving and risk assessment expertiseSalary InsightsCompensation is competitive and aligned with senior regulatory leadership roles within the food manufacturing sector. Final salary depends on experience, technical expertise, and regional exposure.Company OverviewGriffith Foods is a global, family-owned food product development company founded in 1919 and headquartered in Alsip. The company partners with food manufacturers worldwide to develop innovative seasonings, sauces, and coating systems.Guided by its purpose, “We Blend Care and Creativity to Nourish the World,” the organization focuses on sustainability, responsible sourcing, and collaborative innovation across global markets.FAQsIs this a team management role?Primarily an individual contributor role with strong cross-functional influence.Does it involve regional exposure?Yes, the role supports IMEA regulatory and supplier compliance activities.Is prior IMEA experience mandatory?Highly preferred for faster role effectiveness.Application Tips• Highlight supplier documentation and certification management experience• Emphasize regulatory exposure across multiple geographies• Mention audit and compliance system experience• Showcase measurable improvements in supplier quality performance• Demonstrate strong cross-functional coordination examples

Why This Role MattersClinical trials are the foundation of medical innovation. In high-impact therapeutic areas such as Oncology and Immunology, precision, compliance, and patient safety are critical. Every monitoring visit, every data query resolved, and every protocol deviation addressed contributes to the development of potentially life-saving therapies.As a Clinical Research Associate (CRA) II at ICON plc, you play a direct role in ensuring that clinical trials are conducted ethically, safely, and in full compliance with regulatory standards. Your oversight ensures that complex oncology and immunology studies generate reliable data while protecting trial participants. This position is instrumental in advancing innovative treatments from development to regulatory approval.Job DescriptionThe Clinical Research Associate II is responsible for managing and monitoring assigned clinical trial sites in accordance with study protocols, sponsor expectations, ICH-GCP guidelines, and applicable regulatory requirements. This role requires strong on-site monitoring experience, therapeutic expertise in Oncology or Immunology, and the ability to independently manage site relationships.The CRA II acts as the primary liaison between the sponsor and investigational sites, ensuring that studies are conducted with integrity and operational efficiency. The role involves significant travel and requires strong organizational and communication skills to manage multiple responsibilities simultaneously.Key Features of the Role• Focus on Oncology and Immunology therapeutic areas• Independent on-site monitoring responsibilities• Exposure to complex, high-impact clinical trials• Significant travel opportunities (domestic and international)• Cross-functional collaboration with global teams• Career progression toward Senior CRA or Clinical Trial Manager roles• Compliance-driven and patient-focused environmentResponsibilities• Conduct site qualification, initiation, monitoring, and close-out visits in accordance with monitoring plans.• Ensure adherence to study protocols, ICH-GCP standards, and regulatory requirements.• Review source documents to verify data accuracy and completeness.• Ensure informed consent processes are conducted properly and documented accurately.• Monitor patient recruitment, enrollment progress, and retention metrics.• Identify protocol deviations, documentation gaps, and compliance risks.• Ensure timely and accurate reporting of adverse events and safety information.• Perform detailed data review and resolve queries in collaboration with site staff and data management teams.• Ensure case report forms (CRFs) are complete, accurate, and submitted within required timelines.• Collaborate with investigators and site personnel to facilitate smooth trial conduct.• Provide training and support to site staff regarding protocol requirements and study procedures.• Contribute to the preparation and review of essential study documentation, including protocols and clinical study reports.• Maintain accurate monitoring visit reports and follow-up documentation.• Manage multiple sites and ensure all milestones are met within study timelines.Required Qualifications• Strong understanding of clinical trial processes and lifecycle management.• In-depth knowledge of ICH-GCP guidelines and regulatory frameworks.• Proven experience in Oncology and/or Immunology therapeutic areas (mandatory).• Strong analytical skills for interpreting complex clinical data.• Excellent communication and stakeholder management abilities.• High attention to detail and documentation accuracy.• Ability to independently manage site activities and resolve issues proactively.Educational Requirements• Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Medicine, Biotechnology, or related healthcare discipline.• Bachelor’s degree in Life Sciences, Pharmacy• Advanced clinical research certifications are an added advantage.Experience and Skills• Minimum 3 years of experience as a Clinical Research Associate.• Demonstrated on-site monitoring experience.• Experience handling Oncology or Immunology clinical trials (mandatory).• Strong administrative and documentation skills.• Proficiency in Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) platforms.• Experience managing safety reporting and regulatory documentation.• Ability to interpret clinical data and identify trends or discrepancies.• Strong problem-solving and risk mitigation skills.• Ability to work both independently and collaboratively within global teams.• Willingness and ability to travel at least 60% (domestic and international).• Valid driver’s license required.Salary InsightsCompensation for the Clinical Research Associate II role is competitive and aligned with industry benchmarks for Oncology-focused CRA positions. Salary may vary based on therapeutic expertise, travel flexibility, and geographic region.In addition to base salary, employees at ICON plc may receive:• Comprehensive health insurance coverage• Retirement savings programs• Performance-linked incentives• Annual leave entitlements• Life assurance benefits• Global Employee Assistance Programme (LifeWorks)• Flexible lifestyle and wellness benefitsICON’s total rewards framework supports career development, financial planning, and work-life balance.Company OverviewICON plc is a globally recognized leader in healthcare intelligence and clinical research services. The company partners with pharmaceutical, biotechnology, and medical device organizations to accelerate the development of innovative treatments across all phases of clinical development.With a strong presence worldwide, ICON supports complex clinical programs in therapeutic areas including Oncology and Immunology. The organization fosters an inclusive, performance-driven culture focused on scientific excellence and operational quality.Inclusion and belonging are core values at ICON. The company is committed to providing equal employment opportunities and maintaining a workplace free from discrimination and harassment.FAQs1. Is Oncology/Immunology experience mandatory?Yes, therapeutic area experience in Oncology or Immunology is mandatory for this role.2. Does this role require travel?Yes, the position requires approximately 60% travel, including domestic and international visits.3. Is on-site monitoring experience required?Yes, demonstrated on-site monitoring experience is essential.4. What growth opportunities are available?Career progression may include Senior CRA, Lead CRA, Clinical Trial Manager, or Project Management roles.5. Does this role involve data analysis?The role includes data review and query resolution but does not replace formal biostatistical analysis functions.Application Tips• Highlight Oncology/Immunology trial experience prominently in your resume.• Quantify monitoring experience (number of sites, visits conducted, countries supported).• Demonstrate strong knowledge of ICH-GCP and regulatory compliance.• Mention experience handling adverse event reporting and safety oversight.• Emphasize travel flexibility and independent site management capability.• Showcase examples of resolving complex site or data-related issues.