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Clinical Data Svs Associate

Accenture
Accenture
0-3 years
Not Disclosed
10 Dec. 15, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills:

Clinical Data Services Associate

Location: Mumbai, India
Employment Type: Full-Time
Experience Required: 0–3 years
Job ID: AIOC-S01615472
Category: Clinical Data Management | Life Sciences | SAS Clinical


About Accenture

Accenture is a global professional services leader with unmatched expertise in digital, cloud, security, and life sciences consulting. Serving clients across 120+ countries, our 699,000 employees deliver innovative solutions that drive measurable business outcomes. Within our Life Sciences R&D vertical, we provide end-to-end support spanning research laboratories, clinical trials, regulatory services, pharmacovigilance, and patient services, enabling top biopharma companies to improve patient outcomes and accelerate medical innovation.


Role Overview

The Clinical Data Services Associate will support clinical data management projects across the life sciences domain, focusing on high-quality, accurate data collection, processing, and validation. This role is ideal for early-career professionals with exposure to CDISC SDTM standards, SAS programming, and clinical trial data management. You will contribute to data integration, database validation, and clinical study deliverables while maintaining compliance with regulatory guidelines and Accenture’s quality standards.


Key Responsibilities

  • Support clinical data management activities including database validation, edit check creation, and UAT testing.

  • Manage and reconcile clinical data, ensuring accuracy and consistency with CRF/eCRF specifications.

  • Assist with data integration using tools that organize, standardize, and manage clinical research data and metadata.

  • Apply knowledge of trial designs, CDISC SDTM standards, and SAS programming to deliver analytical and operational support.

  • Identify and report protocol deviations, assist in data cleaning, and perform test script execution.

  • Collaborate effectively with internal teams, contributing as an individual contributor while adhering to project timelines.

  • Support rotational shifts as required to meet project or client needs.


Education & Experience Requirements

  • Bachelor’s or Master’s degree in Engineering (BE), Pharmacy (BPharm/MPharm), or related Life Sciences field.

  • 0–3 years of relevant experience in clinical data management, SAS programming, or related life sciences roles.

  • Familiarity with clinical trial processes, data standards, and regulatory requirements is preferred.


Required Skills & Competencies

  • Strong understanding of clinical trial designs, data management workflows, and regulatory standards.

  • Proficiency in SAS programming, CDISC SDTM standards, and clinical databases.

  • Excellent written and verbal communication skills with attention to detail.

  • Ability to work collaboratively in a team environment and manage multiple tasks effectively.

  • Adaptable, flexible, and committed to maintaining high-quality standards in all deliverables.