Pharmacovigilance Jobs: Clarivate is Hiring an Associate Pharmacovigilance Specialist | Apply Now for Clarivate Career
Looking to build your career in the pharma industry and looking for Pharmacovigilance Jobs? Clarivate is hiring passionate life science/ healthcare professionals for the position of Associate Pharmacovigilance Specialist. This full-time hybrid role offers an exciting opportunity to contribute to global biomedical literature monitoring, adverse event reporting, and regulatory compliance while working with a world-class team in Noida or Bangalore. Apply Now and start your professional journey with Clarivate career.
Job Details:
- Job Position: Associate Pharmacovigilance Specialist
- Remote Type: Hybrid
- Locations: R271- Noida, IND – Bangalore (DRG)
- Time Type: Full time
- Job Requisition ID: JREQ134094
Job Description
The Associate Pharmacovigilance Specialist performs pharmacovigilance services such as biomedical literature monitoring and assessing for adverse events reporting, indexing, and abstracting using a broad knowledge of scientific terms and medical terminology, drugs and therapeutic areas, and pharmacovigilance regulations.
About Clarivate:
Clarivate is a global leader in providing trusted insights and analytics to accelerate innovation. The company delivers solutions that empower organizations to discover, protect, and commercialize new ideas. Through advanced data intelligence, technology, and deep domain expertise, Clarivate supports professionals in life sciences, healthcare, academia, and intellectual property sectors.
With a mission to improve the way the world creates, protects, and advances innovation, Clarivate offers industry-leading products and services that drive research, regulatory compliance, and strategic decision-making. Operating across more than 40 countries, Clarivate is committed to fostering diversity, collaboration, and continuous learning — making it an ideal workplace for passionate professionals ready to make a global impact. Through Clarivate career portal, the organizations is providing more Pharma jobs opportunities for the young professionals.
Education:
- Master’s Degree in Life Sciences, Health, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics etc.).
Experience:
- Fresher / Up to 2 years of experience reviewing biomedical literature for adverse event reporting OR equivalent combination of education and experience (i.e., an information science degree with at least 1 year of relevant working knowledge of supporting drug and patient safety).
- Related experience in drug safety/pharmacovigilance is desirable.
- Strong analytic ability to analyze and summarize the main points of biomedical case reports, studies, or specific topics.
- Working knowledge of biomedical terminology, drugs, and therapeutic areas.
- Experience with commercial and client-specific biomedical literature databases.
Additional Skills:
- Certification from a professional medical writer’s association.
- Experience with commercial and client-specific biomedical literature databases.
- Scientific/medical writing background.
- A degree in Dentistry/physiotherapy/Nursing, which involves patient exposure in a hospital-based environment, would be an advantage.
Work Hours
Monday to Friday (Hybrid work model) 12 PM – 9 PM
