Accenture is hiring Clinical Data Services Associates for its Life Sciences R&D vertical in Hyderabad. This opportunity is ideal for B.Pharm graduates with 1–3 years of experience in Clinical Data Management (CDM), eTMF management, and regulated clinical trial documentation.
As part of Accenture’s global clinical operations and regulatory services ecosystem, you will contribute to high-impact clinical trials supporting leading biopharmaceutical companies worldwide.
This role is particularly suitable for candidates aiming to build a long-term career in clinical data services, clinical operations, and regulatory compliance.
🔬 About Accenture
Accenture is a global professional services leader with deep expertise across digital, cloud, security, and life sciences operations. With over 790,000 professionals in 120+ countries, Accenture supports pharmaceutical and biotech organizations across the entire product lifecycle—from clinical trials and pharmacovigilance to regulatory submissions.
🧪 Key Responsibilities – Clinical Data Services Associate
As a Clinical Data Services Associate, your responsibilities will include:
- Supporting Clinical Data Management (CDM) activities such as:
- Discrepancy review and query management
- Data validation and quality checks
- Managing Clinical eTMF (Electronic Trial Master File) lifecycle activities
- Performing accuracy and completeness checks on:
- Trial Master File TOCs
- Protocol packages and amendments
- End-of-trial and essential document checklists
- Assisting with CRF/eCRF review, edit check validation, and UAT testing
- Identifying and escalating protocol deviations
- Supporting eCTD-compliant document formatting, including:
- PDF property checks
- Bookmarking and hyperlink validation
- Good Documentation Practices (GDP) compliance
- Collaborating with global stakeholders to ensure regulatory readiness
🎓 Qualifications & Experience
Required Qualifications:
- Bachelor of Pharmacy (B.Pharm)
Experience:
- 0 to 3 years of experience in:
- Clinical Data Services
- Clinical Data Management
- eTMF Management
- Regulated clinical documentation
Key Skills:
- Strong attention to detail
- Problem-solving and analytical ability
- Ability to work under pressure
- Adaptability in a regulated environment
- Client communication and relationship management
💼 Benefits of Working at Accenture
- Exposure to global clinical trials and regulatory programs
- Structured learning and career growth in Life Sciences R&D
- Competitive compensation and benefits
- Inclusive, diverse, and merit-based work culture
- Opportunity to work with leading biopharma clients worldwide
📌 Salary (Estimated)
- ₹3,50,000 – ₹6,00,000 per annum (based on experience and skills)
Note: Salary may vary based on internal evaluation and Accenture compensation policies.
📝 How to Apply
