CLINICAL DATA SERVICES ASSOCIATE | CLINICAL DATABASE PROGRAMMING | ACCENTURE | BENGALURU
JOB OVERVIEW
The Clinical Data Services Associate role at Accenture is an entry-to-junior level position within Life Sciences Clinical Data Management. The role focuses on supporting clinical trial data operations, database programming, and data validation activities that ensure high-quality clinical research outcomes for global pharmaceutical and biotech clients.
This position involves working with clinical databases, generating data listings, performing edit checks, and supporting end-to-end clinical data review processes used in regulatory submissions and clinical trial reporting.
JOB TYPE
Full-Time | Individual Contributor Role | Rotational Shifts Applicable
LOCATION
Bengaluru, India
EXPERIENCE REQUIRED
0 to 2 years (1 to 3 years preferred depending on project requirements)
QUALIFICATION REQUIRED
Bachelor of Engineering (BE) / Master of Science (MSc)
FUNCTION AREA
Life Sciences R&D | Clinical Data Services | Clinical Database Programming
KEY RESPONSIBILITIES
Support clinical data management activities across global clinical trials
Develop and review edit checks, patient profile listings, and clinical reports
Perform data validation and preprocessing checks to ensure data accuracy
Map and verify clinical datasets based on study-specific requirements
Use tools such as SAS, Cognos, J-Review, and other clinical systems
Assist in Clinical EDC (Electronic Data Capture) design, build, and testing activities
Ensure data consistency, quality, and compliance with study protocols
Support clinical database programming and reporting activities
Collaborate with internal teams for clinical data review and issue resolution
Assist in maintaining regulatory compliance for clinical trial data submissions
SKILLS AND COMPETENCIES REQUIRED
Understanding of Clinical Data Management processes
Knowledge of Clinical EDC systems and database testing
Basic to intermediate skills in clinical programming tools (SAS or similar)
Strong analytical and problem-solving abilities
Ability to manage multiple tasks in a structured environment
Good understanding of clinical trial processes and data workflows
Strong attention to detail and data accuracy
Ability to work in a team-oriented, process-driven setup
Good communication and stakeholder coordination skills
ROLE EXPECTATIONS
Works as an individual contributor within a supervised team structure
Handles routine to moderately complex clinical data tasks
Follows predefined SOPs and detailed instructions for execution
Interacts primarily within internal teams and supervisors
Work output directly impacts assigned deliverables and data quality
May require rotational shift support based on project needs
ABOUT THE ORGANIZATION
Accenture is a global professional services company operating in more than 120 countries. It provides services in Strategy & Consulting, Technology, Operations, and Digital Transformation. Within Life Sciences, Accenture supports pharmaceutical and biotechnology companies with clinical data management, pharmacovigilance, and regulatory services to improve drug development outcomes and patient safety.
NOTE
This recruitment process is transparent and free of charge. Candidates are not required to make any payments at any stage of hiring. All applications are evaluated strictly based on merit and eligibility criteria.
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Remote, India | Siliguri |Illinois :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Copenhagen | Denmark |Europe :
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Netherlands |Remote Australia :
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Harrogate |South Yorkshire :
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Witney |Ontario :
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Argentina | Peru |Brazil :
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