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Clinical Data Svs Associate

Accenture
0-2 years
INR 3.5 LPA – 6 LPA
Bangalore, India
1 June 26, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance

Clinical Data Services Associate

Company: Accenture
Location: Bengaluru, India
Department: Life Sciences R&D – Clinical Data Services
Job Type: Full-Time
Experience: 1–3 Years


JOB OVERVIEW

The Clinical Data Services Associate supports clinical data management activities by developing and validating clinical databases, creating edit checks, generating patient profile listings and reports, mapping datasets, and ensuring high-quality clinical trial data. The role contributes to accurate data collection, validation, and regulatory compliance while supporting clinical research and drug development.


KEY RESPONSIBILITIES

Clinical Data Management

  • Manage and validate clinical trial data.

  • Support clinical database programming activities.

  • Ensure accuracy, consistency, and completeness of clinical data.

  • Perform data validation according to study requirements.

  • Maintain data quality throughout the clinical trial lifecycle.

Clinical Database Programming

  • Develop and review complex edit checks.

  • Create patient profile listings.

  • Generate clinical reports and data listings.

  • Perform preprocessing checks.

  • Map clinical datasets for validation.

  • Configure and maintain clinical databases.

EDC Development & Testing

  • Support Clinical EDC build activities.

  • Participate in Clinical EDC design.

  • Perform clinical database testing.

  • Validate database functionality before deployment.

  • Assist in UAT and quality verification.

Clinical Reporting

  • Generate study-specific reports.

  • Review validation outputs.

  • Support data reconciliation activities.

  • Prepare data extracts for study teams.

  • Ensure reporting accuracy and completeness.

Regulatory Compliance

  • Follow clinical data management SOPs.

  • Maintain compliance with GCP and regulatory guidelines.

  • Ensure audit-ready documentation.

  • Support inspection readiness activities.

Stakeholder Collaboration

  • Work with cross-functional clinical teams.

  • Build strong client relationships.

  • Coordinate with multiple stakeholders.

  • Resolve routine data-related issues.

  • Escalate complex issues when required.


EDUCATIONAL QUALIFICATIONS

Required

  • B.E.

  • M.Sc.


EXPERIENCE REQUIREMENTS

Required

  • 1–3 years of experience in Clinical Data Management or Clinical Database Programming.