Pharmacovigilance Specialist at Clarivate
Position Overview
Job Title: Pharmacovigilance Specialist
Organization: Clarivate
Location: Karnataka, Uttar Pradesh
Salary: ₹8L–₹9L per year
Experience Required: 1-5 years
Qualification: Master’s Degree in Life Sciences, Health or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics, etc.)
About the Role
As a Pharmacovigilance Specialist at Clarivate, you will be integral in analyzing literature citations for individual case safety reports (ICSRs). Your work will impact the risk-benefit and safety profile of our clients’ products by identifying safety-relevant information.
Key Responsibilities
- Literature Analysis: Critically analyze large volumes of biomedical literature and internal drug safety alerts to identify ICSR criteria and safety-relevant information.
- Report Writing: Draft brief narratives summarizing ICSR criteria and other relevant information from each article.
- Drug Safety Review: Conduct drug safety reviews of biomedical literature batches with accuracy and timeliness.
- Database Management: Track actions and assessments in a drug safety system for audit-ready reference.
- Indexing and Abstracting: Write detailed abstracts, create comprehensive indexes, and ensure timely completion of indexing and abstracting in compliance with regulatory deadlines.
- Client Interaction: Utilize knowledge of client’s drug labels during safety assessments and select articles for inclusion in the client’s product literature database.
Qualifications
Required
- Educational Qualification: Master’s Degree in Life Sciences, Health, or Biomedical Sciences (e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics).
- Experience: 1 to 5 years of experience in reviewing biomedical literature for adverse event reporting or an equivalent combination of education and experience.
- Skills: Proficiency in writing succinct, accurate, and precise summaries with a working knowledge of biomedical terminology, drugs, and therapeutic areas.
Preferred
- Certification: Certification from a professional medical writer’s association.
- Experience: Experience with commercial and client-specific biomedical literature databases.
- Background: Scientific or medical writing background.
Skills and Attributes
- Analytical Skills: Ability to critically analyze large volumes of data and literature.
- Communication Skills: Strong writing skills for creating detailed and accurate summaries.
- Knowledge: In-depth knowledge of drug safety, biomedical terminology, and therapeutic areas.
- Attention to Detail: Ensure precise and timely completion of tasks in line with regulatory standards.
Additional Information
- Stay Updated: Remain informed about new drugs, therapeutic categories, disease entities, and changes in biomedical terminology.
- Work Environment: The role is based in Karnataka or Uttar Pradesh, offering a dynamic work environment within a global organization.
Application Process
If you meet the qualifications and are excited about this opportunity, we encourage you to apply. For more details and to submit your application, please visit our
Join Clarivate and be a part of a team dedicated to ensuring the safety and efficacy of pharmaceutical products.