Clinical Data Services Specialist (EDC Build)
Location: Bengaluru, India
Employment Type: Full-Time
Experience Required: 7–11 Years
Job ID: AIOC-S01623119
Function: Clinical Data Management | Life Sciences R&D
Role Overview
We are seeking an experienced Clinical Data Services Specialist to join the Clinical Data Services Team within the Life Sciences R&D vertical. This role is ideal for professionals with strong expertise in Clinical EDC build, database design, and edit check programming, who can lead complex clinical data initiatives and support global biopharma clients across multiple therapeutic areas.
The position plays a critical role in ensuring high-quality clinical trial data that meets regulatory, operational, and scientific standards.
Key Responsibilities
Design, build, and maintain clinical study databases, including electronic Case Report Forms (eCRFs) and edit checks, in accordance with study specifications
Develop and program edit checks, custom functions, and perform unit testing to ensure data accuracy and integrity
Support protocol amendments and database updates through formal change control processes
Manage and support integrations such as IVRS/IWRS, laboratory data, and external vendor data
Ensure clinical trial data compliance with regulatory standards and industry best practices
Collaborate closely with cross-functional teams, sponsors, and stakeholders to meet study timelines and deliverables
Support validation, documentation, and audit readiness activities for clinical data systems
Required Experience & Skills
Experience:
7–11 years of hands-on experience in Clinical Data Services or Clinical Data Management
Minimum 4+ years of experience working with EDC platforms
EDC & Technology Expertise:
Strong experience with EDC systems such as Medidata RAVE EDC, Oracle Clinical, Inform, and Veeva
Proven expertise in:
Database design
Edit check programming
Custom function development
Unit and system testing
Experience with IVRS/IWRS integrations and laboratory data management
Medidata RAVE Study Builder Certification preferred
Professional Competencies:
Strong client relationship management and stakeholder engagement skills
Ability to manage multiple projects and stakeholders simultaneously
Excellent problem-solving, conflict resolution, and decision-making abilities
Proven capability to work under pressure and meet aggressive deadlines
Education
Master of Science (M.Sc) in Life Sciences, Biotechnology, Clinical Research, or a related discipline
About Accenture
Accenture is a global professional services company with leading capabilities in digital, cloud, and security, serving clients across more than 120 countries. Within its Life Sciences R&D practice, Accenture supports the full clinical development lifecycle, including clinical trials, pharmacovigilance, regulatory services, and patient solutions. Accenture combines deep industry expertise with advanced technology to help biopharmaceutical companies accelerate innovation and improve patient outcomes.
Why Join This Role
Work on global clinical trials with leading biopharma organizations
Gain exposure to advanced EDC platforms and clinical data technologies
Be part of a high-impact Life Sciences R&D team driving regulatory-compliant clinical research
Apply now on thepharmadaily.com to advance your career in Clinical Data Services, EDC Build, and Life Sciences R&D Operations.
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