Looking for Pharmacovigilance jobs in Mumbai? Cognizant is hiring experienced professionals for the role of SPE โ Pharmacovigilance. This opportunity is ideal for candidates with 2โ4 years of Pharmacovigilance, Drug Safety, or Clinical Safety experience who want to work with one of the world’s leading healthcare and life sciences service providers.
The role focuses on end-to-end ICSR case processing, safety data review, regulatory reporting, safety signal identification, and compliance with global pharmacovigilance regulations. Professionals with strong knowledge of safety databases, case processing workflows, and regulatory requirements are encouraged to apply.
Job Details
| Particular | Details |
|---|---|
| Company | Cognizant |
| Job Title | SPE โ Pharmacovigilance |
| Job Location | Mumbai |
| Experience | 2โ4 Years |
| Employment Type | Full-Time |
| Work Mode | Hybrid |
| Industry | IT Services & Consulting |
| Department | Research & Development |
Key Responsibilities
As an SPE โ Pharmacovigilance at Cognizant, you will:
- Perform end-to-end pharmacovigilance case processing activities.
- Review clinical trial and post-marketing safety data.
- Analyze adverse event reports and identify potential safety signals.
- Prepare accurate medical narratives and documentation.
- Support regulatory reporting activities.
- Collaborate with medical safety, quality, regulatory, and clinical teams.
- Participate in signal detection and risk assessment activities.
- Ensure compliance with global pharmacovigilance guidelines and SOPs.
- Contribute to continuous process improvements.
- Support internal audits and regulatory inspections.
- Work with pharmacovigilance databases and safety review tools.
- Maintain high-quality safety documentation and case timelines.
Eligibility Criteria
Candidates should possess:
- Degree in Life Sciences, Pharmacy, Medicine, or related discipline
- 2โ4 years of Pharmacovigilance/Drug Safety experience
- Experience in:
- ICSR Case Processing
- Adverse Event Reporting
- Safety Data Review
- Regulatory Reporting
- Drug Safety Operations
- Knowledge of global pharmacovigilance regulations.
- Excellent communication and documentation skills.
- Ability to work with cross-functional global teams.
Preferred Skills
- Pharmacovigilance
- Drug Safety
- ICSR Processing
- Signal Detection
- Risk Assessment
- Clinical Research
- Regulatory Affairs
- Safety Databases
- Medical Review
- Data Management
- Regulatory Compliance
- CTD/eCTD awareness
- SOP Compliance
- Quality Management
Why Join Cognizant?
Working at Cognizant offers:
- Global pharmaceutical projects
- Hybrid work environment
- Career growth in pharmacovigilance
- Exposure to international regulatory standards
- Collaborative healthcare research teams
- Continuous learning and certification opportunities
- Stable long-term career in drug safety
Who Should Apply?
This role is ideal for professionals working as:
- Pharmacovigilance Associate
- Drug Safety Associate
- Drug Safety Specialist
- ICSR Processor
- Safety Scientist
- Pharmacovigilance Executive
- Clinical Safety Associate
How to Apply
