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Associate Pharmacovigilance Specialist

Clarivate
1-2 years
INR 4 LPA – 7 LPA
Karnataka, India
2 June 24, 2026
Job Description
Job Type: Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

ASSOCIATE PHARMACOVIGILANCE SPECIALIST

Company: Clarivate
Location: Karnataka, India
Work Model: Hybrid
Department: Life Sciences & Healthcare

JOB OVERVIEW

Clarivate is seeking an Associate Pharmacovigilance Specialist to support global drug safety and literature surveillance activities. The role involves reviewing biomedical literature, identifying Individual Case Safety Reports (ICSRs), assessing safety-related information, preparing summaries and abstracts, and ensuring compliance with global pharmacovigilance regulations and client requirements.

KEY RESPONSIBILITIES

  • Critically review biomedical literature and internal drug safety alerts to identify Individual Case Safety Reports (ICSRs).

  • Assess published literature for adverse event reporting and safety-related information.

  • Analyze safety findings that may impact the benefit-risk profile of pharmaceutical products.

  • Prepare concise narratives summarizing ICSR criteria and relevant safety information.

  • Review literature batches accurately and within established timelines.

  • Utilize drug safety databases and systems to maintain audit-ready documentation.

  • Select articles for inclusion in client-specific product literature databases.

  • Create detailed scientific abstracts and summaries of selected publications.

  • Extract key scientific findings and prepare comprehensive indexing information.

  • Ensure timely completion of indexing and abstracting activities for regulatory submissions.

  • Maintain awareness of new drugs, therapeutic areas, disease conditions, and biomedical terminology.

  • Support literature searches, terminology maintenance, and additional pharmacovigilance activities as required.

  • Demonstrate understanding of client product labels and apply that knowledge during safety assessments.

EDUCATIONAL QUALIFICATIONS

Required

  • Master’s Degree in:

    • Pharmacy

    • Biotechnology

    • Microbiology

    • Biochemistry

    • Biophysics

    • Biomedical Sciences

    • Life Sciences

    • Health Sciences

Preferred

  • Degree in:

    • Dentistry (BDS)

    • Physiotherapy (BPT/MPT)

    • Nursing

EXPERIENCE

  • 1–2 years of experience in biomedical literature review for adverse event reporting.

  • Experience in drug safety or pharmacovigilance preferred.

  • Experience in scientific writing, literature screening, or medical content review.

  • Knowledge of biomedical terminology, therapeutic areas, and pharmaceutical products.

  • Experience with literature databases and safety information systems preferred.