Accenture Hiring Clinical Data Management & Pharmacovigilance Roles | Freshers Apply Now

Mohit March 18, 2026
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Accenture Hiring Clinical Data Management & Pharmacovigilance Roles | Freshers Apply Now
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Accenture Hiring Clinical Data Management & Pharmacovigilance Roles | 0–3 Years

Accenture
Bengaluru
0–3 Years
Clinical Research
CDM / PV

🏢 About Accenture

Accenture is a global consulting and technology leader operating in 120+ countries. Its Life Sciences division supports pharmaceutical and biotech companies in clinical trials, pharmacovigilance, regulatory operations, and healthcare data analytics.

🔬 Clinical Data Services Associate (Database Programming)

  • Qualification: BE
  • Experience: 1–3 Years
  • Skills: SAS, Cognos, J-Review, EDC

Responsibilities:

  • Develop SAS programs for clinical data analysis
  • Generate listings, tables, and reports
  • Perform database validation and UAT testing
  • Work with EDC systems and clinical databases
  • Ensure CDISC and GCP compliance

📊 Clinical Data Services Associate (Clinical Data Management)

  • Qualification: B.Pharm
  • Experience: 1–3 Years

Responsibilities:

  • Clinical data cleaning and discrepancy management
  • Query generation and resolution
  • CRF/eCRF design and review
  • Database validation and reconciliation
  • Ensure data accuracy and regulatory compliance

💊 Pharmacovigilance Services New Associate (Freshers)

  • Qualification: B.Pharm
  • Experience: Freshers

Responsibilities:

  • ICSR case processing
  • MedDRA coding of adverse events
  • Safety data entry in PV databases
  • Case triage and follow-ups
  • Ensure compliance with PV guidelines

💉 Pharmacovigilance Services Associate

  • Qualification: B.Pharm
  • Experience: 1–3 Years

Responsibilities:

  • End-to-end ICSR processing
  • Narrative writing and case review
  • Regulatory safety reporting
  • Quality checks and compliance
  • Signal detection support

🎓 Eligibility & Skills

  • B.Pharm / BE (relevant fields)
  • 0–3 years experience
  • Knowledge of CDM / PV processes
  • Strong analytical and communication skills
  • Attention to detail

⭐ Salary & Benefits

  • ₹3.5 – ₹7.5 LPA (Estimated)
  • Global pharma project exposure
  • Training in SAS, EDC, safety databases
  • Career growth in clinical research

🎯 Interview Preparation Tips

For CDM Roles:

  • CRF & eCRF design
  • Data cleaning & query management
  • Clinical trial phases

For PV Roles:

  • ICSR workflow
  • MedDRA coding
  • Serious vs Non-serious cases
  • ICH-GCP & GVP basics

Helpful Resources:

📌 Note Before You Apply:
Choose the correct role based on your experience and apply carefully after reviewing job requirements.

👇 Select Role & Apply 👇

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