Accenture is actively hiring for multiple Clinical Data Management (CDM) and Pharmacovigilance (PV) roles in Bengaluru under its Life Sciences R&D vertical. This is a strong opportunity for B.Pharm graduates and BE candidates looking to build a career in clinical research, drug safety, and regulatory services.
With Accenture’s global presence across 120+ countries and deep expertise in clinical trials, pharmacovigilance, and regulatory operations, these roles provide exposure to real-world pharma and biotech projects.
📌 Open Positions
1. Clinical Data Services Associate (Clinical Database Programming)
- Qualification: BE
- Experience: 1–3 years
- Skills: SAS, Cognos, J-Review, EDC Programming
2. Clinical Data Services Associate (Clinical Data Management)
- Qualification: B.Pharm
- Experience: 1–3 years
- Focus: Clinical data validation, lab management
3. Pharmacovigilance Services New Associate
- Qualification: B.Pharm
- Experience: 0–1 years (Freshers Eligible)
4. Pharmacovigilance Services Associate
- Qualification: B.Pharm
- Experience: 1–3 years
💼 Key Responsibilities
Clinical Data Management Roles
- Perform data cleaning, discrepancy review, and query resolution
- Develop edit checks and validation scripts
- Conduct UAT testing and database validation
- Create CRF/ECRF guidelines and SAE reconciliation
- Generate reports using SAS, Cognos, J-Review
Pharmacovigilance Roles
- Handle ICSR case processing (end-to-end)
- Perform MedDRA coding and data entry
- Conduct case triage, follow-ups, and submissions
- Ensure compliance with FDA, EMA, global PV guidelines
🎯 Required Skills
- Clinical Data Management / Pharmacovigilance knowledge
- Strong analytical and problem-solving ability
- Detail-oriented mindset (critical for CDM & PV)
- Ability to work in rotational shifts
- Stakeholder communication & teamwork
🎓 Eligibility Criteria
- B.Pharm / BE (relevant fields)
- 0–3 years of experience depending on role
- Freshers eligible for PV New Associate role
💰 Salary (Expected Range)
- ₹3.5 LPA – ₹7.5 LPA (India, Bengaluru)
(Based on experience and role type)
🌟 Why Join Accenture?
- Global exposure in clinical trials & drug safety
- Work with top pharma & biotech clients
- Strong career path in CDM / PV / Regulatory
- Training in industry tools (SAS, EDC, safety DBs)
- Stable MNC environment with growth opportunities
📍 Job Location
- Bengaluru, India
📩 How to Apply
Application Link For Clinical Data Services Associate (Clinical Database Programming)
Application Link For Clinical Data Services Associate (Clinical Data Management)
Application Link For Pharmacovigilance Services New Associate
Application Link For Pharmacovigilance Services Associate
