Associate Pharmacovigilance
ClinoGenesis Research Institute
This job at a glance
- Who can apply
- Freshers · B.Sc, M.Sc, B.Pharm or Any graduate
- Must know
- Patient careOperationsExcelMicrosoft OfficeOnboarding
- Work
- On-site in Pune City
- Pay
- Not stated by the employer.
- Skill demand
- Operations26%Patient care16%Excel12%Microsoft Office5%of 99 similar fresher jobs posted in India this week
- Listed
- 3 Nov 2026 · still open
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About the Role
Position: Associate Pharmacovigilance (PV)
Company: Clinogenesis Research Organization
Location: Remote
Job Type: Full-time, Entry-Level
About Us
At Clinogenesis Research Organization, we are dedicated to advancing global healthcare through excellence in clinical research, drug safety, and data management. We pride ourselves on nurturing raw talent and providing a launching pad for the next generation of life sciences professionals. We are expanding our Drug Safety team and are looking for enthusiastic, detail-oriented Freshers to join us as Pharmacovigilance Associates.
Key Responsibilities
As a Fresher PV Associate, you will undergo comprehensive training to master drug safety operations. Your daily responsibilities will include:
- ICSR Processing: Review, log, and triage Individual Case Safety Reports (ICSRs) originating from clinical trials, spontaneous reports, and medical literature.
- Data Entry & Triage: Accurately enter adverse event data into global safety databases following strict standard operating procedures (SOPs).
- Medical Coding: Learn and apply MedDRA (Medical Dictionary for Regulatory Activities) and WHO Drug dictionaries for coding adverse events and medications.
- Narrative Writing: Draft clear, concise, and medically accurate case narratives explaining the chronological sequence of adverse events.
- Quality & Compliance: Ensure all cases are processed within strict regulatory timelines mandated by global authorities (FDA, EMA, CDSCO).
Eligibility Criteria
- Education: B.Sc. / M.Sc. / B.Pharm / M.Pharm / Pharm.D or any graduate in Life Sciences (Biotechnology, Microbiology, Biochemistry, Zoology, etc.).
- Graduation Year: 2024, 2025, or 2026 pass-outs with all marks cards cleared.
- Certification: Mandatory certification in Pharmacovigilance / Drug Safety / MedDRA coding
Skills Needed
- Strong understanding of basic human anatomy, physiology, and pharmacology.
- Excellent written and verbal communication skills in English (crucial for narrative writing).
- High attention to detail and strong analytical thinking.
- Basic proficiency in MS Office (Word, Excel).
What’s In It For You?
- World-Class Training: Intensive onboarding program covering global PV regulations, database handling, and medical narrative writing.
- Career Growth: Rapid advancement pathways into Senior PV, Quality Reviewer, or Team Lead roles.
- Culture: A collaborative, supportive, and learning-driven work environment.
- Compensation: Competitive fresher stipend/salary with comprehensive health benefits.