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Clinical Data & Pharmacovigilance Roles
Accenture
Mumbai / Hyderabad / Bangalore
0–3 Years
Clinical Data
Pharmacovigilance
🏢 About Company
Accenture is a global leader in healthcare R&D, working with top pharmaceutical companies in clinical trials, drug safety, and regulatory services.
💼 Clinical Data Services Associate (eTMF)
📌 Responsibilities
- Perform TMF quality review
- Ensure clinical documentation compliance
- Identify data gaps in eTMF
- Support study lifecycle documentation
🎓 Eligibility
- BSc (Life Sciences)
- 1–3 Years experience
💻 Skills
- eTMF systems
- Clinical documentation
- Regulatory basics
- Stakeholder coordination
💼 Pharmacovigilance Services Associate
📌 Responsibilities
- ICSR case processing
- MedDRA coding
- Adverse event reporting
- Safety data review & compliance
🎓 Eligibility
- B.Pharm / M.Pharm
- 1–3 Years experience
💻 Skills
- Drug safety knowledge
- PV regulations
- Case processing tools
- Attention to detail
💰 Salary
- ₹3.5 – ₹7 LPA (Estimated)
🎯 Interview Tips
- Revise eTMF & TMF workflow
- Understand ICSR lifecycle
- Prepare MedDRA hierarchy
- Revise GCP & GVP basics
- Practice scenario-based answers
📌 Note Before You Apply:
Choose the role based on your background (Clinical Data vs Pharmacovigilance) for better chances.
Choose the role based on your background (Clinical Data vs Pharmacovigilance) for better chances.
