Accenture is actively hiring across its Life Sciences R&D vertical for Pharmacovigilance, Clinical Data Management, and Regulatory Affairs roles in India. These roles offer excellent entry-level to mid-level opportunities for B.Pharm, M.Pharm, and Life Sciences graduates.
If you are targeting careers in pharmacovigilance jobs, clinical data management jobs, or regulatory affairs jobs in India, this is a high-value opportunity with a global CRO-like environment.
🔹 Open Positions
1. Pharmacovigilance Services New Associate
📍 Location: Chennai
🧪 Experience: 0–1 years
2. Clinical Data Services Associate (eTMF)
📍 Location: Mumbai
🧪 Experience: 2–4 years
3. Life Sciences Regulatory Services Associate
📍 Location: Bengaluru
🧪 Experience: 1–3 years
4. Clinical Data Services Associate (SAS Clinical)
📍 Location: Bengaluru
🧪 Experience: 0–2 years
🧠 Key Responsibilities
Pharmacovigilance (PV Role)
- ICSR case processing (booking, triage, follow-ups)
- MedDRA coding and safety database entry
- Adverse event detection & reporting
- Regulatory compliance with global PV guidelines
Clinical Data Management (CDM Role)
- eTMF management and document reconciliation
- Data validation, discrepancy management, query resolution
- CRF/eCRF review and database validation (UAT)
- SAE reconciliation and protocol deviation tracking
Regulatory Affairs (RA Role)
- Preparation and submission of regulatory dossiers (eCTD)
- Lifecycle management (CMC, variations, amendments)
- Coordination of global regulatory submissions
- Compliance tracking and audit readiness
🎓 Qualifications
- B.Pharm / M.Pharm / Life Sciences / BSc / BTech / BCA
- Strong understanding of:
- Pharmacovigilance & Drug Safety
- Clinical Data Management
- Regulatory Affairs processes
- Skills:
- Attention to detail
- Communication & documentation
- Analytical thinking
- Ability to work in rotational shifts
💰 Salary (Estimated)
- Freshers (0–1 yr): ₹3.0 – ₹4.5 LPA
- Mid-level (1–4 yrs): ₹4.5 – ₹7.5 LPA
🌟 Benefits
- Global exposure in Life Sciences projects
- Work with top biopharma clients
- Strong career growth in PV, CDM & RA domains
- Structured training & SOP-driven learning
- Opportunity to transition into advanced roles (Signal Detection, SAS Programming, Regulatory Strategy)
🚀 Why This Role Matters
These roles are part of Accenture’s Life Sciences Operations, functioning similarly to a CRO environment (like IQVIA, Parexel, Syneos). You’ll gain hands-on experience in:
- Real-world safety data (ICSRs, MedDRA)
- Clinical trial data lifecycle
- Global regulatory submission processes
This is highly valuable for long-term careers in:
- Pharmacovigilance
- Clinical Research
- Regulatory Affairs
- Data Science in Healthcare
📩 How to Apply
Application Link For Pharmacovigilance Services New Associate
Application Link For Clinical Data Services Associate (eTMF)
Application Link For Life Sciences Regulatory Services Associate
Application Link For Clinical Data Services Associate (SAS Clinical)
