Job Posting: Pharmacovigilance Specialist at Clarivate
About the Company:
Clarivate is looking for a Pharmacovigilance Specialist to perform pharmacovigilance services such as biomedical literature monitoring, adverse events reporting, indexing, and abstracting. This role requires a broad knowledge of scientific terms, medical terminology, drugs, therapeutic areas, and pharmacovigilance regulations.
Position Name:
Pharmacovigilance Specialist
Organization:
Clarivate
Location:
Noida, Uttar Pradesh, India (Hybrid)
Salary:
₹7 Lakhs per year
Experience:
3 years
Qualifications:
- Master’s Degree in Life Sciences, Health, or Biomedical Sciences (e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics)
Job ID:
JREQ125691
Posted Date:
June 19th, 2024
Category:
Life Sciences & Healthcare
What You Will Need:
- Master’s Degree in relevant fields
- At least 3 years of experience in biomedical literature review for adverse event reporting or equivalent combination of education and experience
- Proficiency in writing succinct, accurate summaries with a working knowledge of biomedical terminology, drugs, and therapeutic areas
Responsibilities:
| Task | Description |
|---|---|
| Article Analysis | Critically analyze biomedical literature and internal drug safety alerts to identify ICSRs and safety-relevant information per regulatory requirements and SOPs. |
| Narrative Writing | Write brief narratives summarizing ICSR criteria and other safety-relevant information in each article. |
| Drug Label Knowledge | Use knowledge of client’s drug labels effectively during safety assessments. |
| Review Timeliness | Complete drug safety reviews of biomedical literature batches promptly, adhering to client standards. |
| Tracking Actions | Use the drug safety system to track all actions and assessments in an audit-ready reference history. |
| Article Selection | Select articles specific to the client’s interest for inclusion in their product literature database per guidelines. |
| Abstract Writing | Write accurate, detailed abstracts of selected articles, ensuring excellent organization, grammar, and syntax. |
| Index Creation | Create comprehensive and detailed indexes of abstract contents for precise literature retrieval from the client’s database. |
| Timely Completion | Ensure timely completion of indexing and abstracting for assigned drugs as per regulatory submission deadlines. |
| Awareness Maintenance | Stay updated on new drugs, therapeutic categories, disease entities, and biomedical terminology changes in the published literature. |
| Additional Duties | Participate in other duties like searches and terminology maintenance as needed and per training provided. |
About the Team:
The Pharmacovigilance team at Clarivate serves multiple global customers across all therapeutic areas, offering a supportive working environment with personalized training and engagement opportunities in various aspects of pharmacovigilance.
Hours of Work:
- 11:00 AM IST to 8:00 PM IST, Monday-Friday
- Hybrid work mode: Work from the office at least 2 to 3 days a week, subject to change as per business needs
Equal Employment Opportunity:
Clarivate is committed to providing equal employment opportunities for all persons in compliance with applicable laws and regulations governing non-discrimination in all locations.
Meta Description:
Join Clarivate as a Pharmacovigilance Specialist in Noida. Competitive salary, hybrid work mode, and growth opportunities. Apply now!