If you’re passionate about drug safety, pharmacovigilance, and biomedical literature review, Clarivate is offering an exciting hybrid opportunity for science professionals. As an Associate Pharmacovigilance Specialist, you’ll play a key role in monitoring biomedical data for adverse event reporting—supporting patient safety across the global healthcare ecosystem.
This full-time position, available in Noida and Bangalore, welcomes freshers and professionals with up to 2 years of experience in life sciences, drug safety, or pharmacovigilance.
Key Responsibilities
As an Associate Pharmacovigilance Specialist at Clarivate, your main duties include:
- Reviewing and monitoring biomedical literature for adverse events (AEs).
- Identifying, assessing, and reporting adverse events per pharmacovigilance regulations.
- Performing indexing and abstracting of scientific case reports and studies.
- Summarizing biomedical data with analytical precision and attention to detail.
- Supporting client-specific and commercial literature database management.
- Ensuring compliance with regulatory standards and internal quality systems.
Required Qualifications
To be considered for this role, candidates should have:
- Master’s Degree in Life Sciences, Health Sciences, or Biomedical Sciences (Pharmacy, Microbiology, Biochemistry, Biotechnology, etc.).
- 0–2 years of experience in pharmacovigilance, drug safety, or biomedical literature review.
- Strong command of medical terminology, drugs, and therapeutic areas.
- Analytical skills to evaluate and summarize complex clinical data.
- Familiarity with biomedical databases such as PubMed, Embase, or Medline.
Desirable:
- Certification from a professional medical writer’s association.
- Background in scientific or medical writing.
- Degree in Dentistry, Physiotherapy, or Nursing with hospital experience.
Work Schedule & Location
- Work Type: Hybrid (On-site + Remote flexibility)
- Work Hours: Monday to Friday, 12 PM – 9 PM
- Locations: Noida (R271) and Bangalore (DRG), India
Why Join Clarivate?
At Clarivate, you’ll be part of a global team advancing healthcare safety and innovation. The company values diversity, inclusion, and equal opportunity employment.
Employee Benefits include:
- Hybrid work flexibility
- Career development programs
- Inclusive and supportive work culture
- Opportunity to work on global pharmacovigilance projects
How to Apply
