Looking for Pharmacovigilance jobs in Bangalore? A new opportunity has opened for the role of PSPM Support Associate in Bangalore for candidates with experience in clinical safety, pharmacovigilance, adverse event processing, and post-marketing surveillance.
This role is ideal for candidates from Pharmacy, Life Sciences, Nursing, and Medical Sciences backgrounds who want to build a career in drug safety operations and clinical research. Candidates with experience in adverse event reporting, safety database reconciliation, and clinical trial safety management are encouraged to apply.
Job Details
| Particulars | Details |
|---|---|
| Job Role | PSPM Support Associate |
| Location | Bangalore, India |
| Job Type | Full Time |
| Experience Required | 1+ Years |
| Qualification | PharmD, BS/BA, MS/MA, Life Sciences |
| Industry | Pharmacovigilance / Clinical Safety |
| Last Date to Apply | May 31, 2026 |
Key Responsibilities
The selected candidates will support clinical safety and pharmacovigilance operations related to clinical trials and post-marketing surveillance activities.
Major Responsibilities Include:
- Support Global Safety Leads in clinical safety projects
- Assist in preparation of Safety Management Plans (SMPs)
- Maintain reconciliation plans and safety documentation
- Help in study-specific training, templates, and job aids
- Manage safety database setup and maintenance
- Support adverse event processing and reporting
- Prepare monthly project status reports and metrics
- Assist in Trial Master File (TMF) management activities
- Participate in internal, client, and regulatory audit preparation
- Ensure compliance with pharmacovigilance SOPs and reporting regulations
- Coordinate project-specific training and access management
Required Qualifications
Candidates with the following educational qualifications are eligible:
- PharmD
- B.Pharm / M.Pharm
- BSc / MSc Life Sciences
- Nursing
- Medical Sciences
- Biological Sciences
Experience Criteria
- BS/BA + 1 year relevant experience
- MS/MA + 1 year relevant experience
- PharmD + 1 year relevant experience
- Associate Degree + relevant experience
- Candidates with pharmacovigilance or drug safety exposure preferred
Skills Required
- Knowledge of pharmacovigilance and adverse event reporting
- Clinical safety operations understanding
- Good communication skills
- Attention to detail and accuracy
- MS Office and database management skills
- Ability to work independently and in teams
- Knowledge of global safety reporting regulations
Why Apply for This PSPM Support Associate Role?
This pharmacovigilance job in Bangalore offers exposure to:
- Clinical trial safety operations
- Post-marketing surveillance
- Global drug safety projects
- Regulatory compliance activities
- International pharmacovigilance standards
- Career growth in clinical research and drug safety
Candidates interested in pharmacovigilance jobs for PharmD freshers and experienced professionals can benefit from this opportunity.
How to Apply
