The demand for pharmacovigilance professionals in India continues to rise, and Tata Consultancy Services (TCS) is actively hiring skilled candidates for Drug Safety / PV roles in the Mumbai Metropolitan Region and Pune.

This opportunity is ideal for candidates with 2–5 years of experience in ICSR case processing, Argus database, and drug safety operations, looking to scale their career in a global CRO-like environment.

With increasing regulatory scrutiny and real-world evidence requirements, pharmacovigilance professionals play a critical role in ensuring patient safety and regulatory compliance.

🔬 Job Overview

• Role: Pharmacovigilance Associate
• Company: Tata Consultancy Services
• Location: Mumbai / Pune (On-site)
• Experience: 2–5 Years
• Domain: Drug Safety / Pharmacovigilance
• Work Mode: Full-time
• Application Mode: Email (Immediate Joiners Preferred)

🧪 Key Responsibilities (Pharmacovigilance / ICSR)

• Perform ICSR case processing including data entry, coding, and medical review
• Work on safety databases like Argus Safety for case handling
• Analyze complex clinical safety data and ensure accurate reporting
• Ensure compliance with global pharmacovigilance guidelines (ICH, GVP)
• Execute follow-up procedures for incomplete or missing case information
• Support implementation of patient safety systems and SOPs
• Maintain high-quality case documentation within strict timelines
• Collaborate with cross-functional teams for safety signal management

🎯 Required Qualifications & Skills

• Bachelor’s/Master’s degree in Pharmacy, Life Sciences, or related field
• 2–5 years of experience in pharmacovigilance / drug safety
• Strong knowledge of:
  • ICSR processing workflows
  • MedDRA coding
  • Safety databases like Argus
• Understanding of:
  • ICH-GCP guidelines
  • Global safety reporting requirements
• Excellent communication and documentation skills
• Ability to manage deadlines in a high-volume PV environment

💼 Benefits of Working at TCS

• Opportunity to work with a global life sciences client base
• Exposure to end-to-end pharmacovigilance lifecycle
• Strong learning ecosystem and career growth pathways
• Stable work environment with structured SOPs and compliance systems
• Experience in large-scale safety operations (similar to CRO setups like IQVIA)

📩 How to Apply

Interested candidates (especially immediate joiners) can share their updated CV with the following details:

• Current CTC
• Expected CTC
• Notice Period
• Relevant PV Experience

📧 Email: babeeta.shahi@tcs.com