Clinical Data Services Associate
Job ID: AIOC-S01616459
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Experience Required: 0–2 years (Freshers with relevant exposure may apply)
Education Required: Bachelor of Engineering (BE)
Functional Area: Clinical Data Management | Clinical Database Programming
Industry: Life Sciences | Clinical Research | Healthcare Consulting
Job Overview
Accenture is hiring a Clinical Data Services Associate to support clinical database programming and clinical data management activities within its Life Sciences R&D practice. This role is ideal for early-career professionals looking to build a strong foundation in clinical data operations, EDC systems, and database validation for global clinical trials.
The position offers exposure to clinical database design, edit check programming, data review, and UAT activities, supporting high-quality, compliant clinical research delivery.
Key Responsibilities
Support clinical data management activities, including discrepancy review, query generation, and query resolution.
Assist in developing and maintaining CRF Completion Guidelines (CCG) and SAE reconciliation guidelines.
Identify, document, and track protocol deviations within clinical trial databases.
Develop and review edit checks, preprocessing checks, patient profile listings, and clinical reports based on study requirements.
Create test cases, write test scripts, and support edit check validation and User Acceptance Testing (UAT) for CRF/eCRF systems.
Perform database validation activities to ensure accuracy, consistency, and regulatory compliance.
Support clinical data programming and reporting using tools such as Cognos, SAS, J-Review, or other applicable systems.
Assist in managing clinical data management tasks across multiple studies and timelines.
Required Skills & Competencies
Basic understanding of Clinical Data Management (CDM) and clinical trial processes.
Knowledge or exposure to Clinical EDC design, build, and data review activities.
Familiarity with clinical database programming concepts and validation workflows.
Strong analytical, problem-solving, and attention-to-detail skills.
Ability to work collaboratively and build effective relationships with internal teams and stakeholders.
Good written and verbal communication skills.
Flexible and adaptable to changing project requirements.
Qualifications & Experience
Bachelor of Engineering (BE) is mandatory.
0–2 years of experience in clinical data services, clinical database programming, or related life sciences roles.
Fresh graduates with relevant internships, training, or academic exposure to clinical data management or EDC systems are encouraged to apply.
Role Expectations
Individual contributor role within a structured clinical data management team.
Routine problem-solving using established guidelines and standard operating procedures.
Regular interaction with immediate team members and reporting supervisors.
Moderate to detailed guidance provided for daily tasks and new assignments.
May require working in rotational shifts based on project and study requirements.
About Accenture
Accenture is a global professional services organization with expertise in digital, cloud, security, and intelligent operations, serving clients across more than 120 countries. Its Life Sciences R&D practice supports clinical research, pharmacovigilance, regulatory services, and patient-centric solutions, enabling biopharmaceutical companies to accelerate innovation and improve patient outcomes.
Why Join Accenture
Entry-level opportunity to build a career in Clinical Data Management and Programming
Exposure to global clinical trials and regulated environments
Hands-on experience with EDC systems, validation, and reporting tools
Structured learning, mentorship, and long-term career growth
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