- Full Time
- Bangalore or Noida
Website Clarivate
About Clarivate
Clarivate is a global leader in delivering innovative solutions to accelerate the lifecycle of innovation. Our mission is to empower our customers to solve some of the world’s most complex challenges by providing actionable insights and information. We help clients move from groundbreaking ideas to life-changing inventions, particularly in the realms of science and intellectual property. With our trusted subscription and technology-based solutions, paired with deep domain expertise, we assist customers in discovering, protecting, and commercializing their innovations.
Position: Associate Pharmacovigilance Specialist
Key Responsibilities
As an Associate Pharmacovigilance Specialist, you will play a critical role in pharmacovigilance services by:
- Biomedical Literature Monitoring: Analyzing a large volume of biomedical literature and internal drug safety alerts to identify Individual Case Safety Reports (ICSRs) and other safety-relevant information affecting the risk-benefit profile of customers’ products.
- Safety Assessments: Writing concise narratives summarizing ICSR criteria and other safety-relevant information, leveraging your understanding of client drug labels.
- Timely Reviews: Ensuring the timely, thorough, and accurate review of biomedical literature batches, maintaining high standards of timeliness and quality.
- Audit-Ready Documentation: Using drug safety systems to track actions and assessments, ensuring an audit-ready reference history.
- Literature Database Management: Selecting articles relevant to the client’s interest for inclusion in their product literature database and writing detailed abstracts.
- Indexing and Abstracting: Creating comprehensive indexes of abstract contents to ensure precise literature retrieval from the client’s database, meeting regulatory submission deadlines.
- Continuous Learning: Staying updated on new drugs, therapeutic categories, disease entities, and changes in biomedical terminology.
Candidate Profile
We are looking for candidates who possess:
- A Master’s Degree in Life Sciences, Health, or Biomedical Sciences (e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics).
- 1 to 5 years of experience in reviewing biomedical literature for adverse event reporting, or an equivalent combination of education and experience.
- Strong writing skills for creating accurate and precise summaries.
- A solid understanding of biomedical terminology, drugs, and therapeutic areas.
Additional Information
- Experience: 1 to 5 years
- Qualification: M.Pharm, M.Sc
- Location: Bangalore or Noida
- Functional Area: Life Sciences & Healthcare
- Application Deadline: 30th September, 2024
Join Clarivate and be a part of our bold mission to drive innovation and make a global impact.
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To apply for this job please visit careers.clarivate.com.