Job Title: Clinical Data Services Senior Analyst (CDS Sr Analyst)
Location: Bengaluru, India
Job Type: Full-Time
Experience Required: 5–8 Years
Job ID: AIOC-S01619739
Accenture is a global professional services company with leadership in digital, cloud, and security solutions. With expertise across more than 40 industries, we deliver Strategy and Consulting, Technology and Operations services, and Accenture Song—all powered by a network of Advanced Technology and Intelligent Operations centers. Our 699,000 professionals serve clients in over 120 countries, leveraging technology and human ingenuity to drive transformative outcomes. Visit www.accenture.com to learn more.
The Clinical Data Services Senior Analyst will be aligned with Accenture’s Life Sciences R&D vertical, supporting clinical data operations for leading global biopharma clients. This role focuses on designing, testing, and validating clinical trial databases, ensuring high-quality, compliant data management practices. The CDS Sr Analyst will contribute to EDC database setup, User Acceptance Testing (UAT), edit checks, data extractions, and reporting, supporting accurate evaluation of drug safety and efficacy.
You will work on complex clinical data challenges, collaborate with peers, and occasionally interact with clients or management, while independently managing assigned tasks and small work efforts. This position may require rotational shifts.
Design and test EDC databases in alignment with study requirements
Create and maintain User Acceptance Testing (UAT) procedures for EDC systems
Verify requirements for databases, eCRFs, edit checks, data extractions, and reports
Perform Clinical Database Testing and external data loading activities
Analyze and solve increasingly complex problems in clinical data operations
Maintain data integrity and compliance with regulatory standards
Interact with team members, clients, and management to provide status updates and resolve issues
May oversee a small work effort or team within assigned studies
Strong knowledge of Clinical Data Management (CDM) and EDC systems
Expertise in database testing, UAT, edit checks, and clinical data validation
Familiarity with regulatory standards, SOPs, and industry best practices
Strong analytical, organizational, and problem-solving skills
Excellent written and verbal communication in English
Ability to work independently and collaborate effectively in a team environment
Flexibility to work rotational shifts if required
Bachelor’s degree in Engineering, Life Sciences, or related field (BE/BTech preferred)
5–8 years of experience in clinical data management, database testing, or clinical operations
Proven experience in EDC systems, data validation, and clinical database testing
Gain exposure to global clinical trials across therapeutic areas and phases
Work in a dynamic Life Sciences R&D environment, supporting leading biopharma companies
Enhance your expertise in modern CDM, database validation, and EDC systems
Opportunity for career progression into senior clinical data roles, team lead, or project management tracks
Collaborate with a high-performing team and contribute to life-changing medicines worldwide
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