Instagram
youtube
Facebook

Associate Pharmacovigilance Specialist

1-2 years
Not Disclosed
10 Sept. 24, 2025
Job Description
Job Type: Full Time 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

Job Category:

Life Sciences & Healthcare

Location:

Remote / Hybrid (Available in 2 locations)

Job ID:

JREQ133625

Posted Date:

September 15, 2025


Job Purpose:

Perform pharmacovigilance services including biomedical literature monitoring, adverse event assessment, reporting, indexing, and abstracting, leveraging knowledge of medical terminology, drugs, therapeutic areas, and pharmacovigilance regulations.


Primary Responsibilities:

  • Review biomedical literature for adverse event reporting.

  • Index and abstract biomedical case reports and studies accurately.

  • Assess adverse events and prepare concise, accurate summaries.

  • Utilize broad knowledge of medical terminology, drugs, and therapeutic areas.

  • Maintain compliance with pharmacovigilance regulations and client-specific requirements.

  • Collaborate effectively with team members while maintaining the ability to work independently.

  • Adapt to changing client needs and project priorities.

  • Support creation of pharmacovigilance documentation with high-quality scientific writing.


Required Qualifications:

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

  • Degree in Dentistry, Physiotherapy, or Nursing (hospital-based experience preferred).

  • 1–2 years of experience reviewing biomedical literature for adverse event reporting or equivalent combination of education and experience.

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

  • Strong analytic skills to summarize biomedical case reports and studies.

  • Excellent English comprehension, speaking, reading, and writing skills.

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

  • Basic computer literacy.


Preferred Qualifications:

  • Certification from a professional medical writer’s association.

  • Scientific or medical writing experience.

  • Prior exposure to drug safety or pharmacovigilance operations.


Skills & Competencies:

  • Analytical and critical thinking.

  • Attention to detail and accuracy.

  • Flexibility and adaptability to client requirements.

  • Ability to work independently and collaboratively.

  • Effective communication and documentation skills.


Work Hours:

Monday to Friday – Hybrid work mode


Other Information:

  • Additional duties may be assigned as business needs evolve.

  • Clarivate is committed to equal employment opportunities in all aspects of employment, including hiring, compensation, promotion, and training.