Clarivate Hiring Fresher for Associate Pharmacovigilance Specialist: PV Jobs 2026
Clarivate is hiring fresh graduates (B.Pharm / M.Pharm) for the role of Associate Pharmacovigilance Specialist at its Noida, Uttar Pradesh location. This entry‑level opportunity is perfect for candidates looking to start their career in pharmacovigilance, drug safety monitoring, literature screening, and ICSR processing. As part of Clarivate’s global life sciences team, freshers will gain hands‑on exposure to safety data review, biomedical literature assessment, MedDRA coding, and regulatory‑compliant PV workflows.
Job Overview
- Position: Associate Pharmacovigilance Specialist
- Department: PV
- Location: Noida, Uttar Pradesh, India
- Experience: 0 to 1 Years
- Qualification: B.Pharm, M.Pharm
- Job Type: Full-Time
Key Responsibilities – Associate Pharmacovigilance Specialist
- Literature Screening & Safety Review: Critically review large volumes of biomedical literature and internal safety alerts to identify Individual Case Safety Reports (ICSRs) and other safety‑relevant information in line with regulatory guidelines and SOPs.
- Narrative Writing: Draft brief, clear narratives summarizing ICSR criteria and any potential safety‑related findings identified in each article.
- Drug Label Understanding: Use knowledge of the client’s drug labels and product information to support accurate and consistent safety assessments.
- Timely Batch Review: Perform thorough and timely safety reviews for each assigned literature batch, ensuring accuracy and compliance with Clarivate’s quality standards.
- Documentation in Safety Systems: Record assessments, findings, and actions in the designated drug safety database, ensuring an audit‑ready history of all case‑processing activities.
Required Skills & Qualifications
- Educational Background: Master’s degree in Life Sciences, Health Sciences, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.).
- Experience Level: Open to freshers or candidates with up to 2 years of experience in reviewing biomedical literature for adverse event reporting.
- Candidates with an information science degree plus 1 year of relevant experience in drug or patient safety may also apply.
- Analytical Skills: Strong ability to analyze and summarize key points from biomedical case reports, scientific studies, and research literature.
- Scientific Knowledge: Working understanding of biomedical terminology, commonly used drugs, therapeutic areas, and safety‑related concepts.
- Literature Database Experience: Familiarity with biomedical literature databases (commercial or client‑specific) used for safety monitoring and case identification.
Why Join Clarivate?
Perfect for Freshers Starting Their PV Career
With strong onboarding, structured training, and continuous support, Clarivate is an ideal place for B.Pharm/M.Pharm and Life Sciences graduates to begin their journey in pharmacovigilance and scientific research.
Hands‑On Experience in Drug Safety
You will gain real experience in ICSR identification, literature case review, narrative writing, and MedDRA/drug coding, building a strong foundation for advanced PV roles.
Collaborative Global Work Environment
Clarivate promotes teamwork, transparent communication, and cross‑functional collaboration. You’ll work closely with experienced safety reviewers, analysts, and global clients.
How to Apply
Interested candidates should apply only through the official company career website using the link provided below.
Important Disclaimer
This job post is shared for informational purposes only, based on publicly available job details. Candidates are advised to verify eligibility, job responsibilities, and application procedures from the official IQVIA website before applying.
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FAQ- Associate Pharmacovigilance Specialist
1. Is this role suitable for freshers?
Yes. This role is ideal for B.Pharm, M.Pharm, and Life Sciences freshers, as well as early‑career candidates with up to 2 years of experience in literature screening or drug safety.
2. What will I be doing in this job?
You will screen biomedical literature, identify ICSRs, write brief narratives, perform MedDRA and drug coding, assess safety relevance, and document findings in Clarivate’s safety systems.
3. Do I need prior pharmacovigilance experience?
Not mandatory. Freshers with strong analytical skills and scientific understanding can apply. Clarivate provides role‑specific training.
4. What educational background is required?
A Master’s degree in Life Sciences, Health Sciences, Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, or related fields.
5. What skills are important for this role?
- Ability to analyze biomedical case reports
- Knowledge of medical terminology
- Familiarity with literature databases
- Good communication and documentation skills
- Basic understanding of drugs and therapeutic areas
6. Will I work with global safety databases?
Yes. You will use client‑specific drug safety systems to record case assessments and maintain audit‑ready documentation.
