Accenture Hiring Pharmacovigilance, Clinical Data & QA Roles (1–14 Years)

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Accenture Hiring Pharmacovigilance, Clinical Data & QA Roles (1–14 Years)

✔ Verified by Medical Jobs India

Hiring Pharmacovigilance, Clinical Data & QA Roles 

🏢 Accenture
📍 Bengaluru & Mumbai
🎓 Life Sciences
📊 PV / CDM / QA

Accenture is hiring across Pharmacovigilance, Clinical Data Management, and Quality roles. This is a strong opportunity for freshers to experienced professionals (1–14 years) in clinical research.

👉 Not sure which field to choose? Clinical SAS vs Clinical Data Career Guide

💊 Pharmacovigilance Roles

  • Associate: 1–3 years
  • Sr Analyst: 5–8 years
  • Specialist: 7–11 years
  • Manager: 10–14 years
  • ICSR processing & MedDRA coding
  • Signal detection & safety review
  • Regulatory compliance

📘 Learn PV basics: Pharmacovigilance Practice Quiz

📊 Clinical Data Management Roles

  • Associate: 1–3 years
  • Sr Analyst: 5–8 years
  • Specialist: 7–11 years
  • Data cleaning & validation
  • Database tools (RAVE, SAS)
  • Clinical reporting

📘 Learn CDM: Clinical Data Management Guide

📋 Quality & Compliance Roles

  • Associate Manager: 10–14 years
  • Manager: 13–18 years
  • Audits & inspections
  • CAPA management
  • Quality systems

📘 Learn QA: Quality & Compliance Guides

🎓 Qualifications

  • B.Pharm / M.Pharm
  • MBBS / BDS / MSc / BTech
  • Knowledge of PV / CDM / QA tools

💰 Salary (Estimated)

  • Associate: ₹3.5 – ₹6 LPA
  • Sr Analyst: ₹7 – ₹12 LPA
  • Specialist: ₹12 – ₹18 LPA
  • Manager: ₹18 – ₹30 LPA

💡 Interview Tips

  • Revise GCP guidelines
  • Understand PV/CDM workflows
  • Prepare scenario-based questions
  • Focus on tools (RAVE, MedDRA)

🎯 Practice now: Clinical Quiz Section

🚀 Apply Now

📌 Note Before You Apply: Read full job description carefully before applying.
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