Pharmacovigilance & Clinical Data Management Jobs 2026 | Accenture Hiring PV Associates & Clinical Data Associates

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Pharmacovigilance & Clinical Data Management Jobs 2026 | Accenture Hiring PV Associates & Clinical Data Associates
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Clinical Data Services Associate & Pharmacovigilance Services Associate – Accenture

🏢 Accenture
📍 Bengaluru
🎓 B.Pharm | M.Pharm | BE
💼 Freshers – 3 Years

Accenture is hiring for Clinical Data Services Associate and Pharmacovigilance Services Associate roles in Bengaluru. These opportunities are ideal for candidates interested in Clinical Data Management, Pharmacovigilance, Drug Safety, ICSR Processing, and Clinical Research Operations.

📍 Job 1 – Pharmacovigilance Services Associate

  • Location: Bengaluru
  • Qualification: B.Pharm / M.Pharm
  • Experience: 1–3 Years (Freshers may also apply)
  • Department: Pharmacovigilance & Drug Safety
  • Job Type: Full-Time

📌 Key Responsibilities

  • ICSR Processing
  • Case Intake & Case Identification
  • Adverse Event Review
  • MedDRA Coding
  • Safety Database Entry
  • Case Narrative Writing
  • Duplicate Checks
  • Seriousness & Causality Assessment
  • Follow-up Activities
  • Quality Checks & Compliance Reviews

💡 Required Skills

  • Pharmacovigilance
  • Drug Safety Surveillance
  • ICSR Processing
  • MedDRA Coding
  • Safety Databases
  • Regulatory Compliance

📍 Job 2 – Clinical Data Services Associate

  • Location: Bengaluru
  • Qualification: BE / B.Pharm / M.Pharm
  • Experience: 1–3 Years (Freshers may also apply)
  • Department: Clinical Data Management
  • Job Type: Full-Time

📌 Key Responsibilities

  • Clinical Data Management Activities
  • Medical Monitoring Support
  • Protocol Requirement Review
  • Data Validation & Quality Review
  • Clinical Trial Data Processing
  • Data Consistency Monitoring
  • Clinical Operations Collaboration
  • Regulatory Compliance Support

💡 Required Skills

  • Clinical Data Management
  • Clinical Research Operations
  • Medical Monitoring
  • Protocol Review
  • Data Validation
  • Communication Skills

🎓 Eligibility Criteria

  • B.Pharm
  • M.Pharm
  • BE
  • Healthcare & Life Sciences Background
  • Strong Communication Skills
  • Willingness to Work in Rotational Shifts

🌟 Why Consider Accenture?

  • Global Life Sciences Projects
  • Exposure to Leading Pharma Companies
  • Clinical Research Experience
  • Drug Safety & PV Exposure
  • Clinical Data Management Experience
  • Career Growth Opportunities

💰 Salary & Benefits

Based on current Pharmacovigilance and Clinical Data Management market trends, the estimated salary range is:

💰 Expected Salary: ₹4 LPA – ₹8 LPA

Actual compensation may vary depending on experience, skills, and interview performance.

  • Competitive Salary Package
  • Global Pharmaceutical Project Exposure
  • Career Growth Opportunities
  • Professional Development Programs
  • Healthcare & Insurance Benefits
  • Life Sciences Domain Exposure
  • International Client Interaction
  • Inclusive Work Environment

📈 Pharmacovigilance Career Path

  • Pharmacovigilance Services Associate
  • Drug Safety Associate
  • Senior PV Associate
  • PV Specialist
  • Team Lead – Pharmacovigilance
  • PV Manager
  • Senior Manager – Drug Safety
  • Director – Pharmacovigilance

📈 Clinical Data Management Career Path

  • Clinical Data Services Associate
  • Clinical Data Coordinator
  • Clinical Data Analyst
  • Senior Clinical Data Analyst
  • Clinical Data Manager
  • Lead Data Manager
  • Associate Director – CDM
  • Director – Clinical Data Management

📝 Resume Tips

  • Highlight PV or CDM experience.
  • Mention ICSR processing or data validation work.
  • Include MedDRA coding experience if applicable.
  • Showcase clinical research knowledge.
  • Highlight communication skills.
  • Mention relevant software and databases.
  • Keep resume ATS-friendly.

📌 Before applying, read:

👉 Healthcare & Pharma Application Guide

🎯 Interview Preparation Tips

  • Revise Pharmacovigilance fundamentals.
  • Understand ICSR processing workflow.
  • Review MedDRA coding basics.
  • Revise Clinical Data Management concepts.
  • Understand protocol review processes.
  • Review ICH-GCP guidelines.
  • Research Accenture Life Sciences division.

❓ Common Interview Questions

  1. What is Pharmacovigilance?
  2. What is an ICSR?
  3. What is MedDRA coding?
  4. What is Clinical Data Management?
  5. What is data validation?
  6. What is causality assessment?
  7. What are adverse events?
  8. What is protocol review?
  9. Why do you want to join Accenture?
  10. What are your strengths?

❓ Frequently Asked Questions (FAQ)

Q1. Are freshers eligible?
Yes. Freshers and candidates with up to 3 years of experience can apply.

Q2. Which location is hiring?
Bengaluru, Karnataka.

Q3. Which qualifications are eligible?
B.Pharm, M.Pharm, and BE candidates.

Q4. Are rotational shifts involved?
Yes. Candidates should be comfortable working in rotational shifts.

Q5. Which role is suitable for Pharmacovigilance professionals?
Pharmacovigilance Services Associate.

🚀 Apply – Clinical Data Services Associate

📝 Apply for Clinical Data Services Associate
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