Clinical Data Services Analyst – Life Sciences R&D | Bengaluru, India (Full-Time)
Experience Required: 2–5 years | Qualification: BE / Master of Engineering
Company Overview
Accenture is a global professional services leader specializing in digital, cloud, and security solutions. With operations in over 120 countries and a workforce of 699,000+ professionals, we empower organizations to transform and thrive. Within the Life Sciences sector, Accenture partners with top biopharma companies to deliver clinical, regulatory, pharmacovigilance, and patient-centric solutions. Learn more at www.accenture.com.
Role Overview
The Clinical Data Services Analyst will support Clinical Data Management (CDM) operations in Life Sciences R&D. The role involves database testing, validation, and clinical data analysis to ensure high-quality, accurate, and compliant data collection for clinical trials. This position is ideal for candidates with 2–5 years of experience in clinical data operations or database testing who want to contribute to global clinical research initiatives.
Key Responsibilities
Clinical Data Operations & Testing:
Participate in User Acceptance Testing (UAT) and test case development for clinical databases.
Design, develop, and maintain automated UAT test scripts using tools such as TOSCA.
Execute test cases, analyze results, report defects, and participate in defect resolution and closeout activities.
Conduct pre-dry runs of test cases to ensure accuracy and reliability.
Collaborate with Subject Matter Experts (SMEs) and Business System Owners (BSO) to identify test case scenarios.
Clinical Data Management Support:
Assist in the creation of CRF Completion Guidelines (CCG) and SAE reconciliation guidelines.
Identify protocol deviations in clinical databases and escalate as required.
Perform edit check validation and database validation (UAT) against specified CRF/eCRF requirements.
Participate in regular project meetings and provide updates on UAT timelines and progress.
Collaboration & Documentation:
Communicate findings and status updates to team leads and client stakeholders.
Maintain proper documentation for compliance, audits, and project tracking.
Support process improvements and contribute to team knowledge sharing initiatives.
Candidate Profile
Educational Qualification:
BE or Master of Engineering in a relevant field.
Experience:
2–5 years in clinical data operations, clinical database testing, or related roles.
Skills & Competencies:
Strong analytical and problem-solving skills.
Familiarity with clinical trial data, EDC systems, and clinical database testing.
Ability to work independently and as part of a global team.
Effective communication and collaboration skills with internal and client stakeholders.
Flexible to work in rotational shifts if required.
Why Join Accenture
Work on global clinical trials supporting leading biopharma companies.
Gain exposure to clinical data management, database testing, and validation processes.
Access to continuous learning, certifications, and skill development programs.
Collaborate in a diverse, inclusive, and innovative work environment.
Contribute to projects that directly impact patient outcomes and clinical research advancements.
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Siliguri |Illinois :
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