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PSPM Support Associate
🏢 Fortrea
📍 Bangalore
💊 Pharmacovigilance
💼 0–1+ Years
Fortrea is hiring a PSPM Support Associate for its Pharmacovigilance and Clinical Safety team. This opportunity is ideal for Pharmacy, Life Sciences, Nursing, and Medical Sciences graduates looking to build careers in Drug Safety, Clinical Safety Operations, Adverse Event Reporting, and Post-Marketing Surveillance.
📋 Job Overview
| Particulars | Details |
|---|---|
| Position | PSPM Support Associate |
| Company | Fortrea |
| Location | Bangalore, India |
| Industry | Pharmacovigilance / Clinical Safety |
| Experience | 0–1+ Years |
| Employment Type | Full-Time |
| Last Date | 30 June 2026 |
💊 Clinical Safety & PV Responsibilities
- Support Global Safety Leads on clinical safety projects.
- Assist in preparation of Safety Management Plans (SMPs).
- Support adverse event processing activities.
- Maintain safety documentation and reconciliation plans.
- Support post-marketing surveillance activities.
- Assist with safety reporting and compliance activities.
📑 Documentation & Compliance
- Maintain project-specific safety documentation.
- Support Trial Master File (TMF) activities.
- Assist with study templates and job aids.
- Prepare monthly project metrics and status reports.
- Participate in audit and inspection readiness activities.
- Ensure compliance with PV SOPs and regulations.
⚙️ Project Support Activities
- Manage safety database setup and maintenance.
- Support training coordination activities.
- Assist user access management.
- Coordinate project-specific operational tasks.
- Collaborate with cross-functional safety teams.
🎓 Eligible Qualifications
- Pharm.D
- B.Pharm
- M.Pharm
- B.Sc Life Sciences
- M.Sc Life Sciences
- Nursing
- Medical Sciences
- Biological Sciences
💡 Required Skills
- Pharmacovigilance Fundamentals
- Clinical Safety Operations
- Adverse Event Reporting
- Drug Safety Documentation
- TMF Management
- MS Office Skills
- Regulatory Compliance
- Attention to Detail
- Communication Skills
🌟 Why Join Fortrea?
- Work with a leading global CRO.
- Exposure to global drug safety projects.
- Experience in clinical trial safety operations.
- Career growth in Pharmacovigilance and Clinical Safety.
- Strong learning and development opportunities.
- International clinical research exposure.
📈 Career Path
- PSPM Support Associate
- Drug Safety Associate
- Pharmacovigilance Associate
- Clinical Safety Specialist
- Senior Pharmacovigilance Specialist
- Safety Lead
- Pharmacovigilance Manager
📝 Resume Tips
- Highlight Pharmacovigilance, Drug Safety, or Clinical Research experience.
- Mention adverse event reporting and safety database exposure.
- Include TMF, reconciliation, or clinical trial support activities.
- Showcase attention to detail and documentation skills.
- Mention ICH-GCP and regulatory knowledge if applicable.
- Keep your resume ATS-friendly and achievement-focused.
🎯 Interview Preparation Tips
- Review Pharmacovigilance and Clinical Safety fundamentals.
- Understand adverse event reporting workflows.
- Learn Safety Management Plans (SMPs).
- Review TMF management concepts.
- Understand post-marketing surveillance activities.
- Prepare examples demonstrating teamwork and communication skills.
- Research Fortrea and its global clinical research services.
❓ Common Interview Questions
- What is Pharmacovigilance?
- What is an Adverse Event (AE)?
- What is the role of a Safety Management Plan?
- What is post-marketing surveillance?
- What is TMF and why is it important?
- How do you ensure accuracy in safety documentation?
- What do you know about Fortrea?
- How would you handle multiple project deadlines?
- What is the importance of regulatory compliance in PV?
- Why do you want to work in Drug Safety?
❓ Frequently Asked Questions (FAQ)
Q1. Are freshers eligible?
Candidates with 0–1+ years of relevant experience are encouraged to apply.
Q2. Which location is hiring?
Bangalore, India.
Q3. Which qualifications are eligible?
Pharm.D, B.Pharm, M.Pharm, BSc/MSc Life Sciences, Nursing, Medical Sciences, and Biological Sciences.
Q4. Is Pharmacovigilance experience mandatory?
Relevant drug safety, clinical safety, or pharmacovigilance exposure is preferred.
Q5. What is the last date to apply?
30 June 2026.
📝 How to Apply
- Carefully review the complete job description.
- Update your resume with Pharmacovigilance, Clinical Safety, and Drug Safety experience.
- Highlight adverse event reporting, TMF, and safety documentation exposure.
- Mention clinical research, regulatory, or PV-related projects.
- Apply only if your qualifications align with the role requirements.
👉 Step-by-Step Guide: How to Apply for Healthcare & Pharma Jobs
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📝 How to Apply
- Carefully review the job description.
- Update your resume with Pharmacovigilance, Drug Safety, AE Reporting, and Clinical Research experience.
- Highlight TMF management, reconciliation, and safety operations exposure.
- Apply before 30 June 2026.
- Apply only if your qualifications align with the role requirements.
👉 Step-by-Step Guide: How to Apply for Healthcare & Pharma Jobs
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