Clinical Data Services Senior Analyst
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Experience Required: 2–5 years in Clinical Data Management, SDTM mapping, or Life Sciences analytics
About Accenture Life Sciences
Accenture is a global leader in professional services, delivering unmatched expertise in digital, cloud, and security solutions across 40+ industries. Within Life Sciences, Accenture supports the full spectrum of R&D, from clinical trials and regulatory services to pharmacovigilance and patient services. Our Clinical Data Management (CDM) teams enable leading biopharma companies to transform data into actionable insights, optimizing patient outcomes and supporting innovation. Learn more at www.accenture.com.
Role Overview
We are seeking a Clinical Data Services Senior Analyst to join our Life Sciences R&D team in Bengaluru. The role focuses on managing and analyzing clinical trial data, ensuring accuracy, compliance, and quality in alignment with CDISC, SDTM, and client-defined standards. You will work on data mapping, validation, and quality control while supporting clinical study deliverables and contributing to continuous process improvement.
Key Responsibilities
Review, analyze, and map raw clinical trial data to CDISC and SDTM standards.
Develop annotated case report forms (CRFs) and data definition files aligned with regulatory requirements.
Create and validate edit checks, test cases, and scripts to ensure database accuracy and compliance.
Support discrepancy management, query generation, and resolution across clinical datasets.
Author mapping specifications and quality control outputs for CDISC/SDTM domains.
Assist with project documentation, status reporting, and regulatory submissions.
Collaborate with cross-functional teams to proactively identify and resolve data management issues.
Ensure timely, high-quality deliverables while adhering to internal processes and guidelines.
Required Qualifications & Skills
Bachelor’s degree in Engineering (BE/BTech) or equivalent; Life Sciences/Clinical Data Management exposure preferred.
2–5 years of experience in clinical data management, SDTM mapping, or related clinical data services.
Strong analytical skills, attention to detail, and ability to work under pressure.
Experience with CDISC standards, SDTM mapping, clinical trial data validation, and CRF guidelines.
Proficiency in clinical data management tools, Microsoft Excel, and project documentation.
Adaptable, proactive, and able to solve complex problems independently while collaborating effectively.
Preferred Attributes
Prior experience supporting Life Sciences R&D clients or biopharma projects.
Knowledge of regulatory requirements and clinical trial documentation standards.
Familiarity with data integration, UAT, and SAE reconciliation processes.
Comfortable working in a rotational shift model, if required.
Why Join Accenture
Opportunity to contribute to global Life Sciences projects with leading biopharma clients.
Work in a collaborative, inclusive, and innovative environment that values diversity and professional growth.
Access to learning programs, certifications, and career development opportunities.
Competitive benefits focused on employee well-being, work-life balance, and career progression.
Equal Opportunity & Accessibility
Accenture is an Equal Employment Opportunity Employer. We do not discriminate based on age, race, religion, color, gender, sexual orientation, disability, veteran status, or any other legally protected characteristic. Reasonable accommodations are available for applicants with disabilities during the recruitment process.
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