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About Role & Responsibilities • Dispense medications as per prescriptions • Maintain accurate medication records and inventory management • Ensure the safe and proper storage of pharmaceutical supplies • Provide patient counseling on medication use, side effects, and precautions • Assist in maintaining pharmacy compliance with regulations Qualification • D. Pharm Experience • 0 – 2 years in pharmaceutical dispensing Age Limit • Minimum age: 18 Years • Maximum age: 45 Years • Age relaxation based on organizational norms Selection Process • Interview Application Fee • No application fee Pay Scale • Minimum salary: ₹18,000 per month • Maximum salary: ₹92,300 per month How to Apply • Visit the official JSSC website • Read the notification and check eligibility criteria • Fill out the application form correctly • Attach the required documents • Submit the application form before the closing date Important Dates • Starting date: 08-01-2026 • Closing date: 07-02-2026 About the Company JSSC is responsible for recruiting candidates for various governmental positions in JharkhandOfficial NotificationClick Here
About Role & Responsibilities • Conduct advanced research in the field of pharmaceutical sciences • Assist in the development and execution of scientific studies • Collaborate with multidisciplinary research teams • Prepare research papers, reports, and presentations for publication Qualification • M. Pharm, M.Sc., Pharm D Experience • 3+ years of experience in medical or pharmaceutical research Skills • Strong research and analytical skills • Scientific writing and documentation • Collaboration and team management Age Limit • Minimum age: 18 Years • Maximum age: 45 Years Selection Process • Interview Application Fee • No application fee Pay Scale • ₹73,700 per month How to Apply • Read the instructions carefully and check eligibility criteria • Download the application form • Fill out the application form and attach required documents • Attend the walk-in interview at: Address: Department of Pathology, B-Block, First Floor, Medical College, AIIMS Bathinda Important Dates • Starting date: 20-12-2025 • Closing date: 09-01-2026 About the Company AIIMS Bathinda is a prestigious medical research and education institutionOfficial Notification and Application FormClick Here
About Role & Responsibilities • Conduct inspections of drug manufacturing units and pharmacies • Ensure compliance with drug-related regulations and policies • Take corrective actions in case of violations or discrepancies • Maintain records and reports of inspections and findings • Participate in audits and provide guidance on regulatory requirements Qualification • B. Pharm Experience • 0 – 3 years Age Limit • Minimum age: 21 Years • Maximum age: 45 Years • Age relaxation based on organizational norms Selection Process • Interview Application Fee • No application fee Pay Scale • Minimum salary: ₹44,900/- per month • Maximum salary: ₹1,77,500/- per month How to Apply • Read the instructions carefully and check eligibility criteria • Fill out the online application form • Attach the required documents • Submit the application form before the closing date Important Dates • Starting date: 22-12-2025 • Closing date: 22-01-2026 About the Company UPPSC is the recruitment body responsible for conducting exams and selecting candidates for various government jobs in Uttar PradeshOfficial NotificationClick Here
About Role & Responsibilities • Conduct research in the field of cancer biology • Assist in data collection, analysis, and preparation of research reports • Participate in research discussions and present findings Qualification • Postgraduate degree in Life Sciences or related fields Name of the PostsVacanciesEducationJunior Research Fellow01B.Pharm, PGDM Experience• Freshers / 0 – 2 years of research experience Skills • Research methodologies • Data analysis • Report writing and documentation About the Company ACTREC (Advanced Centre for Treatment, Research and Education in Cancer) is a leading cancer research instituteStarting date16-12-2025Closing date06-01-2026Official NotificationClick Here
About Role & Responsibilities • Dispense medications accurately as prescribed • Maintain patient medication records and ensure proper storage • Provide medication counseling to patients • Monitor and manage the pharmacy inventory Qualification • D. Pharm, B. Pharm Experience • 0 – 2 years in pharmaceutical dispensing Skills • Pharmaceutical dispensing • Patient care and counseling • Inventory management About the Company NIT Puducherry is one of India's premier technical institutions, offering high-quality education and researchStarting date19-12-2025Closing date09-01-2026Official NotificationClick Here
About role & responsibilities • Perform advanced medical coding of diagnoses, procedures and medications • Code clinical trial data using MedDRA and WHO Drug dictionaries • Ensure accuracy, consistency and regulatory compliance across studies • Resolve complex coding discrepancies and medical queries • Collaborate with clinical, safety and data management teams • Support development and refinement of medical coding SOPs and conventions • Stay updated with global medical coding standards Qualification • Bachelor’s degree in Life Sciences, Pharmacy, Healthcare or related field Skills • Strong working knowledge of MedDRA and WHO Drug • Understanding of clinical trial processes and regulatory requirements • High attention to detail and analytical problem-solving skills • Ability to work in cross-functional global teams • Good documentation and communication skills Experience • Proven experience in medical coding within clinical research Salary • ₹6,00,000 – ₹10,00,000 per annum (estimated) Benefits • Comprehensive health insurance for employee and family • Competitive leave entitlements • Retirement and long-term savings plans • Employee Assistance Programme (24/7 wellbeing support) • Life insurance coverage • Flexible benefits – childcare support, gym discounts, travel subsidies and health assessments • Hybrid / office-with-flex work model About the company • ICON plc is a global leader in healthcare intelligence and clinical research • Provides global clinical trial, regulatory and medical coding solutions
About role & responsibilities • Perform triage and initial validity assessment of adverse event cases • Process spontaneous, clinical trial, literature and authority safety reports • Enter safety data accurately into pharmacovigilance databases • Conduct initial ICSR assessments as per global regulatory requirements • Evaluate cases for expedited reporting timelines • Prepare and submit CIOMS I, MedWatch and XML safety reports • Draft and manage follow-up queries to collect missing information • Maintain audit-ready case documentation • Retrieve and review EVWEB company and non-company cases • Support additional pharmacovigilance activities as assigned Qualification • B.Pharm • M.Pharm • BDS • Life Science Graduate Skills • Strong written and verbal communication • High attention to detail • Basic understanding of pharmacovigilance and drug safety reporting • Ability to work within strict regulatory timelines • Willingness to learn global PV regulations Experience • Freshers and early-career professionals can apply Salary • ₹3,00,000 – ₹5,00,000 per annum (estimated) Benefits • Comprehensive training in global pharmacovigilance operations • Exposure to international regulatory standards and safety systems • Career growth within Cencora / PharmaLex • Inclusive and equal-opportunity work culture About the company • Cencora (PharmaLex India Private Limited) is a global healthcare services organization • Focused on pharmacovigilance, regulatory compliance and risk management • Committed to patient safety, diversity and inclusive workplace practices
About role & responsibilities • Assist in pharmaceutical research and development projects • Conduct laboratory experiments and data analysis • Prepare research reports, documentation and presentations • Maintain laboratory records and experimental data • Support faculty and senior researchers in ongoing projects • Ensure compliance with research protocols and institutional guidelines Qualification • M.E / M.Tech • M.Pharm • M.Sc Skills • Research methodology and laboratory techniques • Data analysis and scientific documentation • Good communication and teamwork skills • Basic computer and reporting skills Experience • Freshers and experienced candidates can apply Salary • ₹37,000 per month Benefits • Central government research institute exposure • Fixed monthly stipend • Research learning and career growth opportunities • No application fee Apply • Application start date: 29-12-2025 • Last date to apply: 12-01-2026 About the company • National Institute of Pharmaceutical Education and Research Guwahati is a premier government pharmaceutical institute • Focused on advanced pharmaceutical education and researchOfficial Notification and Apply Online linkClick Here
About role & responsibilities • Support research and development activities under assigned projects • Assist in experimental design, data collection and analysis • Prepare project documentation, reports and presentations • Maintain laboratory records and research data • Coordinate with research teams and faculty members • Ensure compliance with research protocols and institutional guidelines Qualification • M.Pharm • M.Sc • B.Pharm • B.E / B.Tech Skills • Research methodology and documentation • Data analysis and reporting skills • Basic laboratory and technical knowledge • Good communication and coordination skills Experience • Freshers and experienced candidates can apply Salary • ₹42,000 per month Benefits • Government university research exposure • Stable project-based employment • Fixed monthly salary • No application fee Apply • Attend walk-in interview at the address mentioned in the official notification • Walk-in date: 16-01-2026 About the company • Delhi Pharmaceutical Sciences and Research University (DPSRU) is a state government pharmaceutical university • Focused on pharmaceutical education, research and innovationOfficial NotificationClick Here
About role & responsibilities • Work in Life Sciences R&D vertical supporting global pharmacovigilance operations • Create and manage ICSR case identification, data entry, MedDRA coding, case processing, submission and follow-ups • Monitor and assess safety of pharmaceutical products across clinical and post-marketing stages • Ensure compliance with global regulatory requirements and client guidelines • Analyse moderately complex safety data and develop appropriate solutions • Support detection, evaluation and prevention of adverse drug reactions • Manage small teams or work efforts when assigned • Collaborate with internal and client stakeholders • Work in rotational shifts as required Qualification • Bachelor of Pharmacy • Master of Pharmacy • MBBS Skills • Pharmacovigilance operations and ICSR processing • MedDRA coding and safety database management • Regulatory compliance knowledge • Analytical and problem-solving ability • Strong documentation and communication skills Experience • 7 to 11 years of experience in Pharmacovigilance / Drug Safety Salary • Salary Competitive (as per company standards) Benefits • Exposure to global life sciences and pharmacovigilance projects • Career growth and leadership opportunities • Professional and collaborative work environment About the company • Accenture is a global professional services company with strong capabilities in digital, cloud and security • Provides strategy, consulting, technology and operations services across 120+ countries • Serves global biopharma clients through advanced technology and intelligent operations centers
Key Responsibilities Lead and govern global PV safety systems, data marts, UAT and system validation Ensure data integrity, compliance, inspection readiness and regulatory reporting (PSUR, DSUR, PADER) Oversee EDC–Safety DB integrations and reporting solutions (QBE, dashboards) Drive automation, AI adoption and PV process innovation Develop SOPs, training programs and mentor teams Support audits, inspections and QPPV-delegated activities Required Skills & Experience Strong experience with Argus / ArisGlobal LifeSphere Knowledge of global PV regulations, SDLC and system validation Reporting tools: Cognos, Spotfire, Tableau; Oracle DB, PL/SQL, Python preferred Pharma / Health Authority experience mandatory Education Doctorate OR Master’s + 3 yrs OR Bachelor’s + 5 yrs OR Associate’s + 10 yrs OR High School + 12 yrs relevant experience
About the Role Join Accenture’s Life Sciences R&D team to support global drug safety operations. You will process Individual Case Safety Reports (ICSRs) and ensure compliance with international pharmacovigilance regulations. This role is ideal for freshers and early-career professionals entering pharmacovigilance and drug safety. Key ResponsibilitiesProcess ICSRs including case intake, data entry, MedDRA coding, submissions and follow-ups Maintain data accuracy, timelines and audit readiness Ensure compliance with SOPs and global regulatory requirements Support routine pharmacovigilance surveillance activities Eligibility Criteria Educational Qualification Bachelor of Pharmacy (B.Pharm) or Bachelor’s degree in Life Sciences Experience 0 to 1 year of experience (Freshers eligible) Skills Required Basic understanding of pharmacovigilance and drug safety concepts Good attention to detail and data accuracy Ability to follow SOPs and regulatory timelines Basic knowledge of MedDRA coding preferred Good communication and documentation skills Willingness to work in a process-driven, compliance-focused environment
About the Role The Deputy Manager – Pharmacovigilance Safety System (ARGUS) Administrator is responsible for managing and maintaining the safety database infrastructure to ensure compliant, accurate, and efficient pharmacovigilance operations. Key Responsibilities Manage system configuration, user access, workflow setup and system maintenance Monitor compliance and ensure data integrity within the ARGUS safety system Generate and review safety system reports and dashboards Support system validation activities and documentation Provide troubleshooting, user support and training Maintain system-related SOPs, documentation and audit readiness Ensure accurate safety data entry and adherence to regulatory timelines Collaborate with PV operations teams to optimize safety system performance Required Knowledge and Skills Strong understanding of pharmacovigilance regulations including ICH and GVP Knowledge of safety database administration and PV workflows Strong analytical, documentation and troubleshooting skills High attention to detail and organizational ability Excellent communication and training skills Ability to work in compliance with SOPs and quality standards Educational Qualification Bachelor’s or Master’s degree in Life Sciences, Pharmacy or a related discipline About the Company Amneal is a global pharmaceutical organization committed to quality, patient safety and an inclusive workplace culture.
About the Role The Executive – Pharmacovigilance & Drug Safety is responsible for managing signal detection, evaluation, documentation and communication activities to ensure patient safety and regulatory compliance. Key Responsibilities Prepare and maintain signal schedules as per SOPs Identify, analyze and evaluate safety signals from multiple data sources Assess benefit–risk impact and potential label change requirements Prepare product-specific ADR sheets Author Drug Safety Reports for validated signals Communicate signal findings to internal stakeholders Support cross-functional initiatives to enhance pharmacovigilance capabilities Stay updated with global regulatory guidelines related to signal management Ensure compliance with SOPs, timelines and quality standards Assist in development and revision of SOPs, templates and work instructions Deliver signal management training to internal teams Qualification Pharm D / Doctor of Pharmacy Skills and Knowledge Signal detection and evaluation Pharmacovigilance regulations Drug safety reporting Documentation management Strong analytical and communication skills About the Company Amneal is a global pharmaceutical company committed to patient safety, regulatory excellence, and a diverse and inclusive workplace.
About Role & Responsibilities • Perform medical coding for clinical data • Maintain data accuracy • Support healthcare documentation Qualification Graduate / Postgraduate in Life Sciences Experience Freshers / 0 – 2 years Skills • Medical coding • ICD coding • Documentation About the Company Savista is a healthcare information management company
About the role & responsibilities • Act as primary client interface for Safety & Pharmacovigilance services • Lead and manage Safety and PV teams across programs • Oversee delivery as per Safety Management Plans and contracted scope • Monitor quality, KPIs, productivity and drive performance improvement • Ensure timely safety reporting and regulatory compliance • Review study budgets, forecasts and invoicing • Serve as escalation point for sponsors • Lead PV projects and inspections readiness activities • Review protocols, CRFs, SAE forms and safety documents • Develop and approve SOPs, WIs and process improvements • Support business development, bids and proposal reviews • Provide PV training and expert consultation Qualification • Bachelor’s degree in Life Sciences / Pharmacy / Nursing / Healthcare Experience • Extensive leadership experience in Safety & Pharmacovigilance • CRO exposure preferred Skills • ICH-GCP and GVP regulations • Safety reporting operations • People and project management • Budgeting and financial oversight • Strong stakeholder communication About the company • Syneos Health is a global biopharmaceutical solutions organization working on most FDA-approved novel drugs
About the role & responsibilities • Support configuration and optimization of global safety databases • Perform UAT, system validation and safety data integrity checks • Generate and review safety outputs for PSUR, DSUR, PADER, audits and inspections • Configure reports, QBE searches and quality review processes • Support study integrations and EDC–safety database mappings • Drive automation and AI-enabled PV innovations • Develop training, SOPs and support regulatory inspections Qualification • Master’s degree • Bachelor’s degree with relevant PV experience accepted Experience • Pharmaceutical industry / health authority experience mandatory Skills • Argus / LifeSphere safety databases • Aggregate safety reporting (PSUR, DSUR, PADER) • PV analytics and data quality • UAT and system validation • Strong stakeholder communication About the company • Amgen is a global biopharmaceutical leader focused on innovation and patient safety
About Role & Responsibilities • Manage clinical trial documentation • Perform clinical data analysis and reporting • Ensure protocol compliance • Support audits and inspections Qualification B.Pharm / M.Pharm / Pharm.D / MSc / BSc Experience 0–3 years Skills • Clinical data management • Documentation • MS Excel & reporting About the Company TRDFIN provides clinical research and data management services to pharma companies
About Role & Responsibilities • Prepare and maintain regulatory documentation • Coordinate submissions to regulatory authorities • Support product registrations and renewals • Maintain compliance records • Support audit readiness Qualification Bachelor’s / Master’s degree in Pharmacy or Life Sciences Experience 1–4 years Skills • Regulatory documentation • Dossier preparation • Compliance management About the Company Thermo Fisher Scientific delivers scientific solutions across pharma and biotechnology sectors
About Role & Responsibilities • Review central lab and imaging data • Support data analytics and reporting • Maintain quality control of trial data • Coordinate with global study teams • Ensure protocol and regulatory compliance Qualification B.Pharm / M.Pharm / Pharm.D Experience 1 – 4 years Skills • Clinical data management • Centralized monitoring • Regulatory documentation • Reporting tools & analytics About the Company ICON is a leading global CRO delivering high-quality clinical research services worldwide