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Accenture Hiring for CDM, SAS, Pharmacovigilance & eTMF Roles
Accenture
Hyderabad
Mumbai
Chennai
1–3 Years
🏢 About Accenture
Accenture is a global consulting and technology company operating in over 120 countries. Its Life Sciences R&D division supports pharmaceutical, biotechnology, and healthcare companies through clinical trial services, pharmacovigilance operations, clinical data management, and regulatory compliance solutions.
📌 Available Roles
- Clinical Data Services Associate – eTMF Management
- Clinical Data Services Associate – Clinical Data Management
- Clinical Data Services Associate – SAS Clinical
- Pharmacovigilance Services Associate
1️⃣ Clinical Data Services Associate – eTMF Management
Location: Hyderabad
- Manage electronic Trial Master File documentation.
- Perform TMF quality review and completeness checks.
- Maintain regulatory compliant documentation.
- Support clinical trial documentation workflows.
- Ensure compliance with ICH-GCP guidelines.
2️⃣ Clinical Data Services Associate – Clinical Data Management
Location: Mumbai / Hyderabad
- Manage clinical trial data collection and validation.
- Perform data cleaning and discrepancy management.
- Support clinical database review.
- Prepare documentation for clinical study reports.
- Ensure accuracy and integrity of clinical datasets.
3️⃣ Clinical Data Services Associate – SAS Clinical
Location: Mumbai
- Support clinical data integration and analysis.
- Assist with analysis dataset preparation.
- Support cross-study clinical data analysis.
- Assist in clinical statistical reporting.
- Work with SAS tools for clinical datasets.
4️⃣ Pharmacovigilance Services Associate
Location: Chennai
- Process Individual Case Safety Reports (ICSR).
- Perform MedDRA coding for adverse events.
- Maintain pharmacovigilance safety database entries.
- Support safety reporting and follow-up activities.
- Ensure compliance with global pharmacovigilance regulations.
🎓 Eligibility Criteria
- B.Pharm / M.Pharm
- MSc Life Sciences
- BSc Nursing
- Bachelor in Physiotherapy
- BE / Engineering (for SAS role)
Experience: 1–3 Years in Clinical Research / PV / CDM
💰 Salary (Estimated)
₹4.5 LPA – ₹7.5 LPA depending on experience and technical skills.
🎯 Interview Preparation Tips
- Clinical Data Management workflow
- Pharmacovigilance case processing
- Basic SAS clinical datasets
- Trial Master File documentation
Helpful resources:
📌 Select Job Role to Apply
📌 Note Before You Apply:
Kindly read the entire job description carefully before applying.
Kindly read the entire job description carefully before applying.
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