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Associate Pharmacovigilance Specialist

2 years
Not Disclosed
10 Nov. 12, 2025
Job Description
Job Type: Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Pharmacovigilance Specialist

Locations: Available in 2 locations
Department: Life Sciences & Healthcare
Work Mode: Hybrid
Job ID: JREQ134094
Posted Date: October 27, 2025


About the Role

The Associate Pharmacovigilance Specialist is responsible for providing pharmacovigilance services such as biomedical literature monitoring, adverse event assessment and reporting, indexing, and abstracting.
This role requires a strong understanding of scientific and medical terminology, therapeutic areas, and pharmacovigilance regulations.


Key Responsibilities

  • Screen biomedical literature to identify safety information of pharmaceutical products.

  • Assess and report adverse events in compliance with pharmacovigilance regulations.

  • Conduct regular literature reviews to ensure relevant cases are captured and reported.

  • Analyse and summarize the main points of biomedical case reports, studies, and scientific topics.

  • Work with commercial and client-specific biomedical literature databases.


Education and Experience

  • Master’s Degree in Life Sciences, Health, or Biomedical Sciences
    (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)

  • Experience: Fresher or up to 2 years of relevant experience reviewing biomedical literature for adverse event reporting
    (or equivalent education/experience such as an information science degree with relevant exposure in drug safety or patient safety)

  • Prior experience in drug safety/pharmacovigilance is desirable.


Skills and Competencies

  • Strong analytical ability to summarize biomedical data and case reports.

  • Working knowledge of biomedical terminology, drugs, and therapeutic areas.

  • Familiarity with biomedical literature databases.

  • Excellent written communication and attention to detail.


Preferred Qualifications

  • Certification from a professional medical writer’s association.

  • Background in scientific or medical writing.

  • Degree in Dentistry, Physiotherapy, or Nursing (with hospital-based patient exposure).


About the Team

The Pharmacovigilance team at Clarivate includes professionals across India, reporting to respective team managers.
The team combines expertise in market research and consulting, especially within medical devices and healthcare sectors.


Work Hours

  • Shift Timing: 12:00 PM – 9:00 PM (Regular Working Hours)

  • Work Mode: Hybrid


Equal Opportunity Statement

At Clarivate, we are committed to providing equal employment opportunities to all qualified individuals in compliance with applicable laws and regulations.
We ensure non-discrimination in all aspects of employment, including hiring, compensation, promotion, training, and other conditions of work.