Accenture Hiring Clinical Data & Pharmacovigilance Roles | 0–3 Year

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Accenture Hiring Clinical Data & Pharmacovigilance Roles | 0–3 Year
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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.

👇 Select Role & Apply 👇

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