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PSPM Support Associate Pharmacovigilance
🏢 Fortrea
📍 Bangalore
💊 Pharmacovigilance
📑 Clinical Safety Operations
🎓 1+ Years
Fortrea is hiring PSPM Support Associates in Bangalore for candidates interested in Pharmacovigilance, Clinical Safety Operations, Adverse Event Processing, and Post-Marketing Surveillance.
This is an excellent opportunity for candidates looking to build careers in Drug Safety, Clinical Research, Pharmacovigilance Operations, Safety Database Management, and Regulatory Compliance.
📘 Career Guide: Pharmacovigilance Salary Guide India vs USA
📋 Fortrea Recruitment 2026 – Overview
- Position: PSPM Support Associate
- Company: Fortrea
- Location: Bangalore
- Employment Type: Full-Time
- Industry: Pharmacovigilance / Clinical Safety
- Experience: 1+ Years
- Last Date to Apply: 31 May 2026
💰 Estimated Salary: ₹4 – ₹8 LPA
📌 Key Responsibilities
- Support Global Safety Leads in clinical safety projects
- Assist in preparation of Safety Management Plans (SMPs)
- Maintain reconciliation plans and safety documentation
- Support study-specific training and job aids
- Manage safety database setup and maintenance
- Assist in adverse event processing and reporting
- Prepare project status reports and metrics
- Support Trial Master File (TMF) management
- Participate in audits and regulatory inspections
- Ensure compliance with PV SOPs and reporting regulations
📚 Learn Drug Safety Basics: Top Pharmacovigilance Interview Questions
🎓 Eligibility Criteria
- PharmD
- B.Pharm / M.Pharm
- BSc / MSc Life Sciences
- Nursing
- Medical Sciences
- Biological Sciences
📌 Experience Requirements:
- BS/BA + 1 year relevant experience
- MS/MA + 1 year relevant experience
- PharmD + 1 year relevant experience
- Drug Safety / PV exposure preferred
💻 Required Skills
- Knowledge of Pharmacovigilance and AE reporting
- Clinical safety operations understanding
- Good communication skills
- Attention to detail and documentation accuracy
- MS Office and database management skills
- Ability to work independently and in teams
- Understanding of global safety reporting regulations
🧠 Practice Here: Drug Safety Analyst Quiz
🎁 Why Join Fortrea?
- Exposure to global drug safety projects
- Hands-on Pharmacovigilance experience
- Career growth in Clinical Safety & Drug Safety Operations
- International regulatory compliance exposure
- Collaborative CRO work environment
- Learning opportunities in Clinical Research
📚 Learn More About Clinical Research: Clinical Research Career Guide
💡 Interview Tips
- Revise Pharmacovigilance and Drug Safety basics
- Understand AE/SAE reporting workflows
- Prepare questions on ICH-GCP and GVP guidelines
- Practice communication and documentation scenarios
- Understand TMF and safety database concepts
- Be confident discussing internships or PV projects
📊 Interview Preparation: Healthcare Interview Guide
📄 Resume Tips
- Highlight Pharmacovigilance and Clinical Research skills clearly
- Add Drug Safety certifications if available
- Mention internships and safety-related projects
- Keep resume ATS-friendly and professional
- Include communication and documentation skills
- Use clean formatting without spelling mistakes
📚 Career Guidance: Healthcare Career Knowledge Hub
❓ Frequently Asked Questions
- Is this role for freshers? Candidates with 1+ years relevant experience are preferred.
- Which location is hiring? Bangalore.
- What is the main focus of this role? Clinical Safety and Pharmacovigilance Operations.
- What systems will candidates work on? Safety databases, TMF workflows, and AE reporting systems.
- Which backgrounds are eligible? Pharmacy, Life Sciences, Nursing, and Medical Sciences candidates.
🚀 Job Application Link
📌 Important Note Before You Apply:
Please make sure to read the complete job description carefully before submitting your application. Ensure your qualifications, pharmacovigilance knowledge, and clinical safety understanding align with the role requirements before proceeding.
Please make sure to read the complete job description carefully before submitting your application. Ensure your qualifications, pharmacovigilance knowledge, and clinical safety understanding align with the role requirements before proceeding.
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