Pharmacovigilance Specialist Job at Clarivate – Apply Now
Are you an expert in pharmacovigilance and drug safety? Clarivate is hiring a Pharmacovigilance Specialist to perform biomedical literature monitoring, adverse event assessment, and indexing. If you have 4+ years of experience in pharmacovigilance, this is your chance to join a leading global organization that values professional growth and equal opportunities.
Clarivate is committed to providing equal employment opportunities and supports multiple customers covering all therapeutic areas in the pharmacovigilance field. The PV Literature team offers personalized training, a supportive working environment, and opportunities for career growth.
Job Title: Pharmacovigilance Specialist
The pharmacovigilance specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting by using broad knowledge of scientific terms and medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations.
About You
Experience, Education, Skills, and Accomplishments:
- Master’s Degree in Life Sciences, Health, or Biomedical Sciences
- A degree in Dentistry/Physiotherapy/Nursing is advantageous
- At least 4 years of experience in reviewing biomedical literature for adverse event reporting
- Related experience in drug safety/pharmacovigilance is desirable
- Strong analytic ability and writing skills
- Experience in indexing abstracts from literature
Desirable Qualifications
- Certification from a professional medical writer’s association
- Experience with biomedical literature databases
- Scientific/medical writing background
Responsibilities
In this role, you will:
- Analyse biomedical literature and internal drug safety alerts
- Write brief narratives summarizing safety information
- Complete drug safety review promptly
- Index and abstract selected articles accurately
- Maintain awareness of new drugs and therapeutic categories
About the Team
The PV Literature team supports multiple customers and offers a supportive working environment with personalized training. There are opportunities to engage in different aspects of pharmacovigilance and participate in customer upgrade planning.
Hours of Work
This is a full-time permanent position working weekdays (Monday to Friday), 11 am – 8 pm IST.
Keywords: Clarivate, Pharmacovigilance Specialist, Drug Safety Jobs, Biomedical Literature, Medical Terminology
