Clarivate is hiring for the role of Associate Pharmacovigilance Specialist in Bengaluru, offering an excellent opportunity for life sciences graduates with 1โ2 years of experience in pharmacovigilance and biomedical literature review.
This Associate Pharmacovigilance Specialist role is ideal for candidates looking to build expertise in Pharmacovigilance (PV), drug safety, and regulatory-compliant adverse event reporting within a global healthcare intelligence environment.
The position focuses heavily on biomedical literature monitoring, identification of safety signals, and structured scientific summarization aligned with global pharmacovigilance standards.
Job Responsibilities โ Associate Pharmacovigilance Specialist
As an Associate Pharmacovigilance Specialist, your key responsibilities include:
- Performing pharmacovigilance literature monitoring and screening biomedical publications
- Identifying individual case safety reports (ICSRs) from scientific literature
- Summarizing adverse event data into clear, structured narratives
- Indexing and abstracting biomedical articles for safety databases
- Ensuring compliance with global pharmacovigilance regulations and SOPs
- Supporting drug safety teams with timely literature review outputs
- Maintaining accurate documentation in safety tracking systems
- Extracting key findings from clinical and biomedical research articles
- Supporting continuous improvement of PV database quality
This role requires strong analytical ability in Pharmacovigilance Specialist workflows and excellent scientific writing skills.
Required Qualifications
To apply for this Associate Pharmacovigilance Specialist role, candidates should have:
- Masterโs degree in Life Sciences, Pharmacy, Biotechnology, Microbiology, Biochemistry, or related fields
- 1โ2 years of experience in biomedical literature review or pharmacovigilance
- Strong understanding of drug safety and pharmacovigilance concepts
- Experience in scientific writing or medical writing preferred
- Familiarity with biomedical terminology and therapeutic areas
- Excellent English comprehension and writing skills
- Ability to analyze and summarize scientific literature efficiently
Preferred Skills
- Experience in Pharmacovigilance Specialist workflows
- Exposure to biomedical literature databases
- Medical writing or regulatory writing background
- Knowledge of drug safety systems
- Strong attention to detail and compliance mindset
- Adaptability to changing PV requirements
Benefits of Working at Clarivate
Working as an Associate Pharmacovigilance Specialist at Clarivate offers:
- Global exposure in pharmaceutical and healthcare intelligence
- Structured career growth in pharmacovigilance and drug safety
- Opportunity to work with international PV datasets
- Learning environment focused on regulatory compliance
- Professional development in biomedical research and safety reporting
Salary Details
Expected salary for this Associate Pharmacovigilance Specialist role in Bengaluru:
โน4,00,000 โ โน7,00,000 per annum (Approx.)
How to Apply
