Associate Pharmacovigilance Specialist – Clarivate, Apply Now!
Are you passionate about drug safety and pharmacovigilance? Clarivate is looking for an Associate Pharmacovigilance Specialist to support biomedical literature monitoring, adverse event reporting, and regulatory compliance. If you have a background in life sciences and experience in pharmacovigilance or drug safety, this role offers an excellent opportunity to grow your career in a dynamic and supportive environment.
Job Description
The Associate pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by utilizing a broad knowledge of scientific terms, medical terminology, drugs, and therapeutic areas, and pharmacovigilance regulations.
About You
- Master’s Degree in life Sciences, Health, or Biomedical Sciences
- 1-2 years of experience reviewing biomedical literature for adverse event reporting
- Strong analytic ability and writing skills
- Excellent English language skills
Role & Responsibilities:
- Critically analyses large numbers of articles from biomedical published literature and internal drug safety alerts and identifies individual case safety reports (ICSRs) as well as other potential safety-relevant information impacting the risk-benefit and/or safety profile of customer’s products, as per applicable regulatory requirements and standard operating procedures for Associate Pharmacovigilance Specialist role.
- Write brief narratives summarizing the ICSR criteria and other potentially safety-relevant information in each article.
- Demonstrates understanding of client’s drugs labels and uses that knowledge effectively when performing the safety assessments.
- Completes drug safety reviewing of each biomedical literature batch in a timely, thorough, and accurate manner in accordance with client’s standards of timeliness and quality.
- Uses drug safety system to track all actions and assessments in an audit-ready reference history.
- Selects articles specific to client’s interest for inclusion in client’s product literature database per guidelines.
- Writes accurate, detailed, and complete abstracts of selected articles using good judgement regarding the level of detail required and excellent organization, grammar, and syntax preferred for Associate Pharmacovigilance Specialist.
- Extracts key points of articles and creates comprehensive and detailed indexes of the abstract contents to ensure precise and complete retrieval of literature from client’s database.
- Ensures timely completion of indexing and abstracting of articles for assigned drugs in accordance with regulatory submission deadlines.
- Maintains an awareness of new drugs and new therapeutic categories, new disease entities, and changes in biomedical terminology in the published literature.
- Participates in other duties such as searches and terminology maintenance according to business needs and per the training provided.
About the Team for Associate Pharmacovigilance Specialist:
The PV Literature team at Clarivate supports multiple customers covering all therapeutic areas, providing a supportive working environment with personalized training and growth opportunities.
Hours of Work: This is a full-time permanent position working weekdays (Monday to Friday), 11 am – 8 PM IST.
At Clarivate, we are committed to providing equal employment opportunities for all individuals. We comply with applicable laws and regulations governing non-discrimination in all locations.
Keywords: Pharmacovigilance, Biomedical Literature Monitoring, Jobs, Drug Safety, Scientific Terms, Medical Terminology
