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Associate Pharmacovigilance Specialist

1-2 years
Not Disclosed
10 Sept. 18, 2025
Job Description
Job Type: Hybrid Remote Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Job Title: Associate Pharmacovigilance Specialist

📍 Locations: 2 (Hybrid – Remote)
🆔 Job ID: JREQ133625
📅 Posted Date: September 15, 2025
🏢 Business Unit: Life Sciences & Healthcare


Role Overview

The Associate Pharmacovigilance Specialist is responsible for performing pharmacovigilance services such as biomedical literature monitoring, assessment of adverse events for reporting, indexing, and abstracting. The role requires broad knowledge of scientific and medical terminology, therapeutic areas, drugs, and pharmacovigilance regulations.


Education & Qualifications

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

  • Advantage: Degree in Dentistry, Physiotherapy, or Nursing with hospital-based patient exposure

  • Certification from a professional medical writer’s association (preferred)


Experience

  • Required:

    • 1–2 years reviewing biomedical literature for adverse event reporting OR equivalent education/experience (e.g., Information Science degree + 1 year relevant experience)

    • 1+ year experience in summarizing biomedical case reports/studies

    • 1+ year working knowledge of biomedical terminology, drugs, and therapeutic areas

    • Experience with commercial/client-specific biomedical literature databases

    • Strong English communication skills (reading, writing, speaking, comprehension)

  • Desirable:

    • Related experience in Drug Safety / Pharmacovigilance

    • Scientific/medical writing background


Key Skills

  • Strong analytical skills to interpret and summarize complex biomedical information

  • Excellent writing skills for clear, precise, and accurate summaries

  • Knowledge of biomedical terminology, therapeutic areas, and drug safety practices

  • Familiarity with literature databases and indexing systems

  • Flexibility to adapt to changing client needs

  • Ability to work independently and collaboratively

  • Basic computer literacy


Work Hours & Mode

  • Monday to Friday

  • Hybrid Work Mode


Additional Information

  • Job responsibilities may evolve with changing business needs. Additional duties can be assigned.

  • Equal Employment Opportunity: Clarivate is committed to inclusion, diversity, and non-discrimination in all aspects of employment, in compliance with applicable laws and regulations.


Impact: This role ensures accurate monitoring and reporting of biomedical literature, directly supporting drug safety and patient safety in compliance with global pharmacovigilance standards.