Looking for Pharmacovigilance jobs in Mumbai? Glenmark Pharmaceuticals Limited has announced an exciting opportunity for experienced Pharmacovigilance professionals. The company is hiring an Officer – Pharmacovigilance for its R&D division in Navi Mumbai. Candidates with experience in ICSR processing, clinical trial safety, SAE reconciliation, and pharmacovigilance operations are encouraged to apply.
This Pharmacovigilance job at Glenmark offers exposure to global safety operations, clinical trials, regulatory compliance, and collaboration with cross-functional teams across the pharmaceutical industry.
About Glenmark Pharmaceuticals
Glenmark Pharmaceuticals Limited is a leading global pharmaceutical company focused on innovation, research, and development. The organization operates across multiple therapeutic areas and is known for maintaining high standards in drug safety, pharmacovigilance, and regulatory compliance.
Job Details
| Particulars | Details |
|---|---|
| Company | Glenmark Pharmaceuticals Limited |
| Position | Officer – Pharmacovigilance |
| Department | Pharmacovigilance |
| Location | Mahape, Navi Mumbai, Maharashtra |
| Experience | 2–3 Years |
| Qualification | M.Pharm, B.Pharm, Master’s Degree in Health Sciences |
| Employment Type | Full-Time |
| Salary | ₹5,00,000 – ₹6,50,000 per annum |
| Job ID | Job_2564 |
Key Responsibilities
Clinical and Safety Operations
- Collaborate with clinical project teams on safety-related activities.
- Participate in clinical and safety review meetings with Medical Monitors.
- Ensure consistency in safety assessments and SAE follow-up activities.
- Support preparation of Safety Management Plans (SMPs).
- Assist with clinical safety regulatory submissions.
Pharmacovigilance Case Management
- Ensure timely receipt and processing of Individual Case Safety Reports (ICSRs).
- Support adverse event reporting activities.
- Follow up on serious adverse event (SAE) cases.
- Maintain compliance with pharmacovigilance reporting timelines.
SAE Reconciliation Activities
- Participate in reconciliation between clinical and safety databases.
- Coordinate with Data Management teams.
- Support data lock reconciliation activities.
- Resolve reconciliation queries and discrepancies.
Documentation and Compliance
- Maintain Trial Master File (TMF/eTMF) documentation.
- Support Inspection Safety Master File (ISMF) management.
- Ensure proper archiving and filing of pharmacovigilance records.
- Maintain compliance trackers and safety documentation.
Process Improvement and Oversight
- Manage pharmacovigilance mailboxes.
- Perform safety website monitoring activities.
- Support SOP development and implementation.
- Contribute to compliance initiatives and audits.
Eligibility Criteria
Candidates applying for this Pharmacovigilance Officer job should possess:
Educational Qualification
- M.Pharm
- B.Pharm
- Master’s Degree in Health Sciences
Experience Required
- 2–3 years of Pharmacovigilance experience.
- Hands-on experience in ICSR processing.
- Experience handling clinical trial safety cases.
- Knowledge of SAE reconciliation processes.
Required Skills
- Strong written and verbal communication skills.
- Excellent proofreading abilities.
- Knowledge of pharmacovigilance regulations.
- Working knowledge of Microsoft Outlook, Word, Excel, and PowerPoint.
- Experience using electronic document management systems.
- Ability to handle confidential medical information.
- Understanding of ICH, FDA, and global safety reporting requirements.
Why Join Glenmark?
- Opportunity to work in global pharmacovigilance operations.
- Exposure to clinical trial safety management.
- Collaboration with regulatory affairs and clinical teams.
- Career growth in drug safety and pharmacovigilance.
- Competitive salary and professional development opportunities.
How to Apply
