Job opportunity for Pharmacovigilance Specialist @ Clarivate- Apply before 30th January 2024


Website Clarivate

About Clarivate

Clarivate, a company that specializes in accelerating the innovation lifecycle. Clarivate’s mission is to assist customers in addressing complex global challenges by offering valuable information and insights that facilitate the transition from innovative ideas to transformative inventions in the fields of science and intellectual property. They achieve this goal by helping customers discover, safeguard, and monetize their innovations through a combination of reliable subscription and technology-driven solutions, all backed by their extensive domain knowledge and expertise.

Job Post: Pharmacovigilance Specialist

Job Description:

Position Summary: The pharmacovigilance specialist plays a vital role in monitoring biomedical literature, assessing adverse events, and ensuring compliance with pharmacovigilance regulations. Utilizing in-depth scientific knowledge, the specialist contributes to the identification and reporting of safety-related information affecting the risk-benefit profile of client products.

Duties and Responsibilities:

  • Analyze biomedical literature for adverse event reporting and identify individual case safety reports (ICSRs).
  • Write concise narratives summarizing ICSR criteria and safety-relevant information.
  • Utilize knowledge of client’s drug labels for effective safety assessments.
  • Complete drug safety reviews in a timely and accurate manner, adhering to quality standards.
  • Maintain an audit-ready history using the drug safety system for tracking actions.
  • Select and include articles of client interest in the product literature database.
  • Write accurate abstracts with attention to detail and excellent organization.
  • Extract key points, creating comprehensive indexes for precise literature retrieval.
  • Ensure timely completion of indexing and abstracting for regulatory submissions.
  • Stay informed about new drugs, therapeutic categories, and changes in biomedical terminology.
  • Participate in additional duties such as searches and terminology maintenance.

Candidate Profile:

  • Master’s Degree in life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.).
  • Dentistry/physiotherapy/Nursing degree with hospital exposure is advantageous.
  • 2-4 years of experience in biomedical literature review for adverse event reporting.
  • Relevant experience in drug safety/pharmacovigilance is desirable.
  • Strong analytical ability and writing skills for concise summaries.
  • Working knowledge of biomedical terminology, drugs, and therapeutic areas.


  • Excellent English language skills (comprehension, speaking, reading, and writing).
  • Proficiency in biomedical terminology, drugs, and therapeutic areas.
  • Experience with commercial and client-specific biomedical literature databases.
  • Flexibility and adaptability to changing client needs.
  • Ability to work effectively, independently, and collaboratively.
  • Basic computer literacy.

Additional Information:

  • Experience: 2-4 years
  • Qualification: Master’s Degree in life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)
  • Location: Noida, UP
  • Industry Type: Pharma / Healthcare / Clinical research
  • End Date: 30th January 2024
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