Accenture is actively hiring across its Life Sciences R&D division for Clinical Data Services Associate and Pharmacovigilance (PV) Associates, including Japanese language PV roles. These openings are ideal for candidates with 0–3 years of experience in clinical research, drug safety, and data management.
If you’re targeting careers in clinical data management, eTMF, or pharmacovigilance, this is a strong entry point into a global organization.
🔹 Open Positions (Updated Titles for SEO)
- Clinical Data Management Associate – eTMF Specialist (Mumbai)
- Pharmacovigilance Associate – Drug Safety & ICSR Processing (Chennai/Bengaluru)
- Pharmacovigilance Associate – Japanese Language Specialist (Chennai)
- Pharmacovigilance New Associate – Freshers (Bengaluru)
🔬 Key Responsibilities
Clinical Data Services (eTMF Role)
- Perform Trial Master File (TMF) quality review
- Validate clinical trial documents and ensure compliance
- Support clinical data lifecycle (collection, validation, reconciliation)
- Work with TMF Manager on document accuracy and completeness
- Manage protocol packages, checklists, and study reports
Pharmacovigilance Roles
- Process ICSRs (Individual Case Safety Reports)
- Perform MedDRA coding
- Case intake, follow-up, and submission to global databases
- Ensure compliance with regulatory requirements (FDA, EMA, etc.)
- Handle safety data from clinical trials and post-marketing
Japanese PV Roles
- Handle Japan market safety cases
- Apply JLPT (N3–N5) language skills in case processing
🎓 Qualifications
- Bachelor’s degree in Life Sciences / B.Pharm / M.Pharm
- Experience: 0–3 years
- Strong understanding of:
- Clinical trials / eTMF systems
- Pharmacovigilance workflows
- For Japanese roles: JLPT N3–N5 certification preferred
💼 Skills Required
- Stakeholder management
- Attention to detail (critical for TMF/PV compliance)
- Ability to work under pressure and meet deadlines
- Analytical thinking in clinical data review
- Team collaboration in global delivery models
💰 Salary (Estimated)
- ₹3.2 LPA – ₹6.5 LPA (based on role, location, and experience)
🌟 Why Join Accenture Life Sciences?
- Work with top global pharma clients
- Exposure to clinical trials, regulatory, and drug safety domains
- Strong career progression in CDM, PV, and Regulatory Affairs
- Global delivery model experience
- Training in industry-standard tools (Argus, Arisg, Veeva, etc.)
📍 Job Locations
- Mumbai (Clinical Data – eTMF)
- Chennai (PV & Japanese PV roles)
- Bengaluru (PV roles – freshers & experienced)
📌 How to Apply
Application Link For Clinical Data Svs Associate – TMF
Application Link For Customer Service Associate – Japanese PV
Application Link For Customer Service Associate – Japanese PV
Application Link For Pharmacovigilance Services Associate
Application Link For Pharmacovigilance Services Associate
Application Link For Pharmacovigilance Services New Associate
