Looking for a Pharmacovigilance job in Bangalore? Clarivate is hiring an Associate Pharmacovigilance Specialist for its Bangalore location. This is an excellent opportunity for candidates with experience in drug safety, biomedical literature review, adverse event reporting, and pharmacovigilance operations.
Candidates with a Master’s degree in Life Sciences, Pharmacy, Biotechnology, Microbiology, Biochemistry, or related biomedical sciences with 1–2 years of pharmacovigilance experience are encouraged to apply.
This Associate Pharmacovigilance Specialist job in Bangalore offers exposure to global drug safety processes, biomedical literature monitoring, ICSR case assessment, and medical writing activities.
Job Overview
| Details | Information |
|---|---|
| Job Title | Associate Pharmacovigilance Specialist |
| Company | Clarivate |
| Location | Bangalore |
| Job Type | Full-Time |
| Work Mode | Hybrid |
| Experience Required | 1–2 Years |
| Qualification | Master’s Degree in Life Sciences / Pharmacy / Biomedical Sciences |
| Department | Pharmacovigilance / Drug Safety |
| Working Days | Monday to Friday |
| Shift | 9 Hours |
Key Responsibilities – Associate Pharmacovigilance Specialist
The selected candidate will be responsible for handling pharmacovigilance and biomedical literature monitoring activities including:
- Reviewing biomedical literature for adverse event reporting
- Identifying and processing Individual Case Safety Reports (ICSRs)
- Writing concise medical narratives and safety summaries
- Monitoring drug safety alerts and risk-benefit information
- Maintaining audit-ready documentation in drug safety systems
- Indexing and abstracting biomedical literature articles
- Supporting regulatory compliance and pharmacovigilance SOP adherence
- Extracting key scientific and therapeutic information from literature
- Managing client-specific biomedical literature databases
- Supporting literature searches and terminology maintenance activities
This role is ideal for professionals seeking career growth in pharmacovigilance jobs for pharmacy graduates and drug safety associate roles in India.
Required Qualifications
Candidates applying for this Clarivate Pharmacovigilance job should possess:
Educational Qualification
- Master’s Degree in:
- Pharmacy
- Biotechnology
- Microbiology
- Biochemistry
- Biomedical Sciences
- Biophysics
- Life Sciences
Preferred Background
- Dentistry
- Physiotherapy
- Nursing with hospital exposure
Experience
- Minimum 1–2 years experience in:
- Biomedical literature review
- Pharmacovigilance operations
- Drug safety case processing
- Medical writing
Preferred Skills
The company is looking for candidates with:
- Strong understanding of biomedical terminology
- Knowledge of therapeutic areas and drug safety regulations
- Excellent scientific writing and English communication skills
- Experience with commercial biomedical literature databases
- Analytical and summarization skills
- Flexibility to work on client-specific requirements
Candidates with medical writing certifications or prior pharmacovigilance database exposure will have an added advantage.
Why Join Clarivate?
Working with Clarivate provides professionals an opportunity to build expertise in:
- Global Pharmacovigilance Operations
- Biomedical Literature Surveillance
- Drug Safety & Regulatory Compliance
- Medical Writing & Scientific Abstracting
- International Healthcare Data Management
Employees also benefit from a hybrid work environment and exposure to global pharmaceutical clients.
Salary Expectations
Based on industry standards for Associate Pharmacovigilance Specialist jobs in Bangalore, the expected salary range is:
- ₹4.5 LPA – ₹7 LPA
Actual compensation may vary depending on experience, skillset, and interview performance.
How to Apply
