Non Clinical Jobs Jobs

Roles & Responsibilities• Monitor investigator sites using risk-based monitoring (RBM)• Ensure compliance with protocol, ICH-GCP, SOPs, and regulations• Conduct site initiation, monitoring, and close-out visits• Perform SDV, SDR, and CRF reviews for data accuracy• Maintain essential documents and audit readiness• Communicate with sites, sponsors, and project teams• Prepare monitoring reports, follow-up letters, and status updatesQualification• Bachelor’s degree in Life Sciences or Registered NursingExperience• 2+ years of experience as a Clinical Research MonitorSkills• Strong knowledge of ICH-GCP and clinical trial regulations• Proficiency in MS Office and CTMS toolsAbout The CompanyThermo Fisher Scientific is a global leader in serving science, providing innovative solutions for life sciences, diagnostics, and applied materials. With a strong commitment to supporting researchers and healthcare professionals, Thermo Fisher offers a comprehensive range of tools and services that enable the advancement of scientific discovery.

Roles & Responsibilities• Write and review regulatory medical writing documents such as protocols, clinical study reports (CSRs), narratives, informed consent documents (ICDs), and clinical overviews and summaries• Develop slide decks and website content related to regulatory writing• Support primary clinical manuscripts, literature reviews, abstracts, posters, and other related materials• Collaborate with cross-functional teams to ensure accuracy and compliance with regulatory guidelines• Ensure timely delivery of high-quality medical writing contentQualification• Degree or Postgraduate in Life SciencesExperience• 10+ years in Regulatory Medical WritingSkills• In-depth knowledge of regulatory writing processes and requirements• Strong writing and editing skills with attention to detail• Experience with clinical documentation and submission processes• Ability to work collaboratively within cross-functional teams• Proficient in scientific writing and document preparationAbout The CompanyKrystelis Ltd is a leading organization specializing in regulatory medical writing services. With a focus on compliance and quality, Krystelis works on diverse clinical and regulatory writing projects, helping clients navigate the complexities of medical documentation.

Roles & Responsibilities• Conduct medical services and provide support to clinical teams• Manage and lead medical affairs and marketing strategies• Support the development of scientific publications and materials• Ensure compliance with regulatory guidelines in medical services• Collaborate with internal teams for product development and marketing• Provide medical and scientific expertise to support strategic initiativesQualification• MD – PharmacologyExperience• 0–3 yearsSkills• Strong knowledge in medical affairs and pharmacology• Excellent communication and interpersonal skills• Ability to interpret scientific data and apply it to medical services• Proficient in medical writing and scientific presentationsAbout The CompanyAlembic Pharmaceuticals Ltd. is a leading pharmaceutical company committed to providing high-quality products and services. With a strong presence in the medical industry, Alembic focuses on innovation and compliance, aiming to improve the lives of patients worldwide.

Roles & Responsibilities• Handle pharmacy operations and ensure the availability of medicines• Oversee medication dispensing and ensure proper storage• Monitor inventory levels and manage procurement for the pharmacy• Provide pharmaceutical care and counseling to patients• Ensure compliance with PCI and hospital standards• Collaborate with healthcare providers for effective patient careQualification• D.Pharm / B.Pharm• Valid Telangana PCI RegistrationExperience• Freshers may applySkills• Strong knowledge of pharmaceutical practices and medication management• Excellent communication and interpersonal skills• Ability to manage inventory and handle procurement• Good organizational skills and attention to detailAbout The CompanyAnkura Hospital for Women & Children, Hyderabad, is committed to clinical excellence and providing quality healthcare to women and children. As part of our growth, we are expanding our pharmacy department and are seeking dedicated professionals who share our vision for patient care and operational excellence.

Roles & Responsibilities• Oversee the planning, execution, and completion of clinical research projects.• Manage project timelines, resources, and compliance with research protocols.• Coordinate with different departments and stakeholders to ensure successful project delivery.Qualification• MSc with Post Graduate Diploma in Clinical Research (mandatory) or MSc-Clinical Research.Experience• Experience in clinical research project management.Skills• Strong project management skills, including planning, resource allocation, and team coordination.• In-depth knowledge of clinical research processes.• Ability to handle complex tasks and meet deadlines.About The CompanyTata Memorial Centre is a global leader in cancer research and treatment. The institution focuses on providing comprehensive cancer care and advancing research to improve patient outcomes.

Roles & Responsibilities• Drive scientific excellence in the rapidly evolving Hepatology space• Engage with key opinion leaders and healthcare professionals• Support evidence-based clinical practice with robust scientific communication• Collaborate with cross-functional teams to deliver medical insights and strategic supportQualification• MBBS / MD (Pharmacology)Experience• Freshers and experienced candidates are welcome to applySkills• Strong scientific communication• Collaboration skills• In-depth knowledge in Hepatology• Ability to engage and work with healthcare professionals and key opinion leadersAbout The CompanyDr. Reddy’s Laboratories is a global pharmaceutical company, dedicated to providing high-quality medicines in the form of innovative solutions for patients worldwide. Dr. Reddy’s Laboratories focuses on bringing science and medicine together to improve patient care.

Roles & Responsibilities:• Manage reception and telephone duties as the first point of contact• Provide dental assisting support when necessary (no experience required)• Coordinate practice schedules and appointments• Liaise between the practice, patients, specialists, and laboratories• Assist with administrative and basic clinical duties as required• Maintain cleanliness and appearance of reception and common areas• Ensure smooth daily operations and deliver a welcoming patient experienceQualifications:• Previous reception experience in a professional firm preferred (2+ years)Experience:• Minimum 2 years of reception experience preferred• Dental assisting experience not requiredSkills:• Strong communication and interpersonal skills• Excellent attention to detail and accuracy• Confident, vibrant, and professional demeanor• Strong computer proficiency• Excellent time management and prioritisation abilities• Mature, self-aware, and team-oriented• Driven to learn and grow professionallyBenefits:• Continuing education opportunities (internal and external)• Supportive and stable team environment• Opportunity to develop communication and people skills• Rewarding role contributing to patient health and wellbeingAbout the Company:Oasis Dental is a modern dental practice dedicated to redefining the dental experience. The clinic focuses on high-quality care that not only addresses dental issues but also prevents future problems, delivering a superior standard of treatment in a supportive and professional environment.

Roles & Responsibilities:• Regulatory query management and responses• Scientific and technical justification preparation• Compliance and regulatory documentation• Cross-functional coordination with internal teams• CAPA handling and continuous improvement activities• Maintaining confidentiality and ethical standardsQualification:• M.Pharm in Regulatory AffairsExperience:• 3 to 5 years in Regulatory Affairs (Pharma)Skills:• Expertise in regulatory query management• Strong scientific and technical writing skills• Familiarity with compliance and regulatory documentation• Ability to work cross-functionally• Strong attention to detail and confidentialityAbout the Company:Accuprec Research Labs Pvt. Ltd. is a leading contract research organization (CRO) dedicated to providing regulatory, clinical research, and pharmaceutical solutions to the global healthcare market. Based in Ahmedabad, Gujarat, the company specializes in regulatory affairs and aims to ensure compliance with all relevant standards and regulations.

Roles & Responsibilities:• Assist Principal Investigator (PI) in site feasibility assessments• Support pre-trial documentation and regulatory readiness• Collect and maintain updated CVs of site staff• Ensure timely completion of financial disclosure forms, PI undertaking, and confidentiality agreements• Coordinate with IRB/IEC for faster approvals and timely submission of safety reports and protocol amendments• Assist PI & Co-Investigators in Informed Consent Process• Prepare for Site Initiation Visits (SIV)• Maintain Site Master File (SMF) and patient files• Handle patient recruitment, screening, enrollment, and follow-ups• Complete CRF and clinical data entry• Coordinate patient follow-up visits (physical & telephonic)• Report and follow-up on SAE (Serious Adverse Events)• Manage drug accountability and inventory tracking• Maintain study budget sheets and track IRB fees, site administration fees, lab costs, and patient reimbursementsQualification:• B.Pharm, M.Pharm, Pharm.D, Msc, BSc, LifesciencesExperience:• 1–4 years in clinical research / clinical trialsSkills:• Knowledge of ICH-GCP Guidelines• Experience with IRB/IEC Submissions• SAE Reporting & Drug Safety• CRF Completion & Clinical Data Management• Patient Recruitment & Site CoordinationAbout The Company:Max Healthcare is one of India’s leading hospital networks, offering an advanced research ecosystem for clinical trials. The company is focused on providing comprehensive healthcare and pioneering clinical research that adheres to global standards, promoting patient safety and the highest standards of care.

Roles & Responsibilities:• Perform hands-on, in-house repairs on dental equipment including control units, curing lights, milling machines, and diagnostic devices• Conduct component-level fault finding on PCBs, control boards, and electrical assemblies• Diagnose mechanical and electrical faults using schematics, manuals, and test equipment• Support on-site servicing and installations, including setup, calibration, and functional testing• Communicate professionally with dentists and clinic staff during field visits• Ensure all work meets quality, safety, and compliance standards• Accurately record service activity in systems such as SAP and Salesforce• Collaborate with customer service teams, contractors, and internal technicians• Participate in ongoing technical training and product upskillingQualifications:• Restricted Electrical Licence (mandatory)• Electrical Disconnect/Reconnect Licence or X-ray equipment licence desirableExperience:• Relevant hands-on repair experience is essential• Proven experience working on PCBs, electrical control units, and electronic assemblies• Experience in medical or dental equipment advantageous but not required• Backgrounds in high-tech automotive systems, electrical switchboards, industrial electronics, IT hardware, or complex electronic devices consideredSkills:• Strong troubleshooting and fault-finding capability• Ability to work autonomously in a repair or service environment• Confident communication skills with professional customer interaction• Ability to work within regulated, quality-driven environments• Strong teamwork and collaboration skillsAbout the Company:Healthcare Professionals Group is a global provider of dental equipment and consumables, supporting clinics and laboratories across Australia. Known for integrity, long-term stability, and strong customer focus, the company delivers high-quality technology used daily by dental professionals while fostering a supportive and collaborative work culture.

Roles & Responsibilities:• Greet patients warmly and manage appointment schedules, including booking and confirmations• Update and maintain patient records with strong attention to detail• Handle phone calls and enquiries efficiently in a high-volume environment• Assist with general administrative tasks to support smooth practice operations• Work closely with the clinical team to ensure efficient daily patient flowQualifications:• Proficient experience in Medical or Dental Reception highly preferredExperience:• Prior experience in a medical or dental reception role preferredSkills:• Strong multitasking abilities with the capacity to work in a fast-paced environment• Excellent customer service and professional communication skills• Reliable, adaptable, and team-oriented• High attention to detail in patient records and data entryAbout the Company:Smile Partners Australia is a growing network of specialist orthodontic practices dedicated to creating confident smiles using the latest technology. The organization combines clinical excellence with a supportive and collaborative culture.

Roles & Responsibilities• Teach Pharmacology to BDS students through lectures, tutorials, and practical sessions as per prescribed curriculum• Guide students on rational drug use, prescription writing, and pharmacology relevant to dental practice• Prepare lesson plans, teaching materials, and academic schedules• Conduct internal assessments, evaluations, and assist in university examinations• Maintain academic records, attendance, and assessment documentation• Participate in departmental academic activities, seminars, and curriculum development• Engage in research activities, publications, and scholarly work (preferred)• Ensure compliance with DCI/NMC norms and university regulations• Support overall academic growth and quality standards of the institutionQualification• MD in Pharmacology from a recognized medical college as per NMC/DCI norms• Valid State Medical Council / NMC registrationExperience• Relevant teaching experience as per the designation norms prescribed by NMC/DCI• Research and publication exposure is preferredSkills• Strong subject knowledge in Pharmacology• Effective teaching, presentation, and communication skills• Ability to mentor and guide undergraduate dental students• Academic planning, documentation, and assessment skills• Research orientation and publication interest• Commitment to regulatory compliance and academic excellenceAbout the OrganizationThe institution is committed to delivering quality dental education aligned with national regulatory standards, focusing on academic excellence, research, and holistic professional development of students.

Roles & Responsibilities• Perform batch documentation review and support batch release activities for products listed on Aspire Pharma’s MIA and third-party MIAs• Review stability data and ensure compliance with approved specifications• Manage deviations, non-conformances, CAPAs, and change control activities• Support MIA product setup, batch release documentation, and launch readiness activities• Conduct monthly compliance checks and contribute to product launch activities• Maintain up-to-date knowledge of EU/UK GxP regulations, including GMP, GDP, GVP, and GCP• Ensure compliance with regulations related to medical devices (ISO 9001, ISO 13485, ISO 14971), controlled drugs, nutritional products, GDPR, and the UK Data Protection Act• Communicate effectively with internal teams, vendors, and customers to implement regulatory changes• Investigate non-conformances and deviations and support corrective and preventive actions• Monitor vendor performance to ensure compliance and supply continuity• Update quality procedures and documentation in line with legislative and regulatory requirementsQualification• Bachelor’s degree in Science or related disciplineExperience• 5–8 years of relevant experience in Quality Assurance or Technical Compliance (desirable)• Experience with MIA batch review and release activities (desirable)• Strong understanding of pharmaceutical regulatory and compliance requirementsSkills• Excellent written and spoken English communication skills• Strong time management and organizational abilities• High attention to detail and documentation accuracy• Proactive team player with problem-solving mindset• Proficiency in MS Office (Word, Excel, Outlook)• Experience with Adobe Acrobat and electronic signature tools (desirable)• Familiarity with Q-Pulse or other electronic QMS systems (desirable)About the CompanyAspire Pharma is a UK-based asset-light pharmaceutical manufacturer with a diversified portfolio of over 250 products across urology, ophthalmology, CNS, dermatology, and specialty generics, delivering innovative and reliable healthcare solutions to underserved markets worldwide.

Roles & Responsibilities• Assist in preparation and review of aggregate safety reports, risk management plans, and signal detection activities• Generate outputs and reports from safety databases and systems• Support data requests, sales data calculations, regulatory website searches, and report planning activities• Author full or partial sections of global regulatory safety documents, including: Annual Reports (IND and others), PSUR / PADER / PBRER, DSUR, Risk Management Plans (RMPs)• Develop assigned report sections using templates, reused content, and low to medium complexity safety analyses• Review and annotate line listings, prepare case narratives, and summarize safety data per approved strategies• Participate in comment resolution and report finalization discussions• Support signal detection activities, including data cleaning, line listing review, and preparation of signal review materials• Assist in preparing ad hoc safety reports, safety issue analyses, and label update justifications• Write sections of Common Technical Document (CTD) summaries, including Clinical and Non-Clinical Overviews• Conduct literature searches and screen publications for relevance to safety reports• Prepare literature abstracts and summaries for regulatory documentation• Ensure compliance with SOPs, regulatory requirements, GVP, and ICH-GCP guidelines• Promote consistent, efficient, and high-quality writing processes to meet project timelines• Maintain high standards of customer service and effective collaboration with internal and external stakeholdersQualification• Bachelor’s degree in Life Sciences or equivalent• Advanced degree (Master’s or PhD) preferredExperience• Excellent written and spoken English skills• Strong organizational and time management abilities• Scientific or clinical research experience is desirable• Knowledge of pharmacovigilance, regulatory requirements, and ICH-GCP guidelines preferred• Around 2 years of experience in medical writing or the pharmaceutical industry is an advantageSkills• Proficiency in MS Word, PowerPoint, and Excel• Strong analytical and documentation skills• Ability to manage multiple deliverables under timelines• Excellent interpersonal and communication skillsAbout the CompanyFortrea is a leading global clinical research organization providing end-to-end clinical development and safety solutions, supporting pharmaceutical and biotechnology companies worldwide.

Roles & Responsibilities:• Support global safety literature screening for ICSR identification and signal detection• Perform pharmacovigilance literature surveillance as per regulatory requirements• Screen and review literature (articles, abstracts, citations) for safety information• Triage literature for GSK marketed and development products using defined criteria• Support periodic reporting and signal detection activities• Maintain up-to-date product knowledge and master drug lists• Perform quality checks on triaged literature and ensure documentation accuracy• Collaborate with PV, Medical Affairs, and Regulatory teamsQualification:• Bachelor’s degree in Life Sciences / Pharmacy / Pharmacology / Medical disciplineExperience:• 1–5 years of experience in literature review, pharmacovigilance support, or medical writing• Pharmaceutical industry experience preferred (Drug Safety / Regulatory / Clinical / Medical Affairs)Skills:• Working knowledge of pharmacovigilance regulations and methodologies• Strong scientific literature searching and screening skills• Good understanding of medical and scientific terminology• Excellent attention to detail and analytical skills• Strong communication, interpersonal, and teamwork skills• Good computer skills and experience with web-based applicationsAbout the Organization:GSK is a global biopharmaceutical company focused on vaccines and specialty medicines, uniting science, technology, and talent to get ahead of disease together while prioritizing patient safety and public health.

Roles & Responsibilities:• Assist in processing Individual Case Safety Reports (ICSRs)• Perform adverse event (AE) and serious adverse event (SAE) case intake• Support case triage, data entry, and quality checks• Ensure compliance with global pharmacovigilance regulations• Work with medical terminologies such as MedDRA and WHO-DD• Maintain accurate drug safety documentation• Collaborate with senior drug safety associates and PV teamsQualification:• M.Pharm / B.Pharm / PharmD / MSc Life SciencesExperience:• Freshers onlyNo. of Openings: 30Skills:• Basic understanding of Pharmacovigilance and drug safety processes• Awareness of adverse events and clinical pharmacology• Familiarity with medical terminology• Good attention to detail and willingness to learnAbout the Organization:The company is a global pharmaceutical organization with established pharmacovigilance operations, offering freshers hands-on exposure and a strong foundation in drug safety and clinical safety operations.Interested and eligible candidates should share their updated CV to email: sahana.s@randstad.in

Roles & Responsibilities:• Lead and manage Quality Assurance activities across API and pharmaceutical manufacturing• Oversee implementation and compliance of cGMP, GLP, and quality management systems• Review and approve SOPs, BMRs, validation documents, and quality reports• Drive deviation management, CAPA effectiveness, change control, and risk assessments• Lead internal audits and support regulatory inspections (US FDA, WHO, CDSCO, EDQM)• Ensure data integrity, audit readiness, and continuous improvement initiatives• Coordinate with Production, QC, Regulatory Affairs, and cross-functional teams• Mentor, train, and develop QA team members; manage workload and performanceQualification:• B.Pharm / M.Pharm /M.Sc (Chemistry, Microbiology, or relevant discipline)Experience:• 10+ years of experience in Quality Assurance (Pharma / API)• Mandatory team handling and leadership experienceSkills:• Strong expertise in cGMP, GLP, and global regulatory requirements• Proven experience in regulatory audits and inspections• Excellent leadership, decision-making, and stakeholder management skills• Strong documentation, compliance, and problem-solving abilitiesAbout the Organization:Arch Pharmalabs is a reputed API manufacturing company with globally compliant facilities, offering leadership roles with strong exposure to international regulatory standards and continuous improvement initiatives.

Roles & Responsibilities:• Oversee quality assurance activities across API and pharmaceutical manufacturing• Conduct audits, inspections, and documentation reviews as per cGMP standards• Handle deviations, CAPA, change control, and risk management activities• Ensure compliance with regulatory guidelines (US FDA, WHO, CDSCO, etc.)• Coordinate with Production, QC, and cross-functional teams for quality improvements• Prepare, review, and maintain SOPs, BMRs, and validation documents• Support regulatory inspections, audits, and submissions• For Managerial roles: Lead QA teams, mentor staff, and drive continuous improvement initiativesQualification:• B.Pharm / M.Pharm /M.Sc (Chemistry, Microbiology, or relevant discipline)Experience:• Officer / Executive: 3–8 years in QA (Pharma / API)• Manager / Sr. Manager: 10+ years including team handling experienceSkills:• Strong knowledge of cGMP, GLP, and quality management systems• Experience in deviation management, CAPA, and change control• Exposure to regulatory audits (US FDA / EDQM / WHO preferred)• Excellent documentation, communication, and coordination skillsAbout the Organization:Arch Pharmalabs is a reputed API manufacturer with globally compliant facilities, offering strong career growth and exposure to international regulatory standards.

Roles & Responsibilities:• Partner with Global Study Leaders to monitor study conduct, progress, risks, timelines, and budgets• Support end-to-end operational study delivery from study set-up to close-out and archival• Maintain and ensure completeness of study systems, trackers, databases, and project plans• Review key clinical documents (Protocol, ICFs) and support development of monitoring, vendor, risk, and deviation management plans• Coordinate cross-functional study team communication, meetings, and documentation• Act as primary point of contact for country oversight activities including recruitment, data completeness, deviations, and local budgets• Manage vendor and CRO oversight, ensuring delivery of study-specific deliverables• Oversee clinical supplies, investigational products, and study materials; escalate supply risks proactively• Ensure eTMF inspection readiness through setup, periodic review, and follow-up on missing or quality issues• Support financial activities including change orders, expense tracking, and budget consistency across systemsQualification:• Bachelor’s degree in Life Sciences or related disciplineExperience:• Relevant experience in clinical trial coordination, study operations, or global study delivery• Experience working in FSP, CRO, or sponsor environments preferredSkills:• Strong knowledge of clinical trial operations and study lifecycle• Experience with eTMF oversight, vendor/CRO management, and country coordination• Good understanding of ICH-GCP and regulatory requirements• Strong project management, risk management, and analytical skills• Excellent communication, coordination, and stakeholder management skills• Ability to work in a global, cross-functional environmentAbout the Organization:The organization is a global biopharmaceutical leader advancing vaccines and innovative medicines, offering FSP professionals global exposure, end-to-end study ownership, and strong career growth opportunities in clinical research.