Accenture Hiring Pharmacovigilance, Clinical Data, Regulatory & SAS Roles | 0–4 Years

Mohit April 01, 2026
📢 For Latest Job Updates
📲 Join WhatsApp Channel 💼 Follow on LinkedIn
Accenture Hiring Pharmacovigilance, Clinical Data, Regulatory & SAS Roles | 0–4 Years
✔ Verified by Medical Jobs India

Pharmacovigilance, Clinical Data, Regulatory & SAS RolesAccenture

Chennai / Mumbai / Bangalore
0–4 Years
PV / CDM / RA / SAS

🏢 About Company

Accenture Life Sciences R&D works with global pharma and biotech companies across pharmacovigilance, clinical trials, regulatory affairs, and data analytics. It offers strong exposure to CRO-like environments and global healthcare projects.

1️⃣ Pharmacovigilance Services New Associate

  • Location: Chennai
  • Experience: 0–1 Years (Freshers Eligible)
  • Key Work: ICSR processing, MedDRA coding, safety reporting

2️⃣ Clinical Data Services Associate (eTMF)

  • Location: Mumbai
  • Experience: 2–4 Years
  • Key Work: eTMF management, data validation, query resolution

3️⃣ Life Sciences Regulatory Services Associate

  • Location: Bangalore
  • Experience: 1–3 Years
  • Key Work: eCTD submissions, lifecycle management, compliance

4️⃣ Clinical Data Services Associate (SAS Clinical)

  • Location: Bangalore
  • Experience: 0–2 Years
  • Key Work: Clinical data analysis, SAS basics, validation

🎯 Interview Preparation Tips

  • Revise ICH-GCP & clinical trial lifecycle
  • Prepare ICSR & MedDRA concepts
  • Understand eTMF & regulatory basics
  • Learn SAS basics (PROC, DATA step)
  • Be ready with practical examples

Helpful Resources:

📌 Note Before You Apply:
Kindly select the role based on your experience before applying.

👇 Select Role & Apply 👇

🔎 More Pharma Jobs
📲 Join for Instant Updates
Tags