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Clinical Data Services Associate

Accenture
Accenture
0-2 years
preferred by company
Bangalore, India
1 May 14, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data Services Associate
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Department: Clinical Data Management / Clinical Research / Life Sciences R&D
Experience Required: 0–2 Years (Freshers with relevant technical qualifications may be considered)


Job Overview

An exciting opportunity is available for a Clinical Data Services Associate within the life sciences and clinical research domain. This role is ideal for professionals looking to build expertise in clinical data management, clinical database programming, EDC systems, clinical trial data validation, and regulatory-compliant research operations.

The selected candidate will support clinical data services across the clinical research lifecycle, ensuring accurate collection, validation, storage, analysis, and reporting of clinical trial data. This role plays a crucial part in supporting pharmaceutical and biopharmaceutical research by maintaining high-quality data used to assess treatment safety and efficacy.

This position is well-suited for early-career professionals seeking growth in clinical data management, clinical technology, life sciences R&D, and biopharma operations.


Key Responsibilities

Clinical Data Management

  • Support collection, validation, processing, and management of clinical trial data
  • Ensure clinical data accuracy, completeness, consistency, and regulatory compliance
  • Maintain high-quality study data for safety and efficacy evaluation
  • Assist in data integrity monitoring throughout the clinical research lifecycle

Clinical Database Programming & Validation

  • Develop and review edit checks based on study-specific requirements
  • Support clinical database testing and validation activities
  • Prepare patient profile listings, reports, preprocessing checks, and validation datasets
  • Perform data mapping and verification to maintain accurate clinical datasets

Clinical EDC Support

  • Assist with Clinical EDC (Electronic Data Capture) build and design activities
  • Support implementation of study database configurations
  • Help maintain clinical systems and workflow accuracy

Clinical Research Operations

  • Collaborate with teams supporting clinical trials, pharmacovigilance, and regulatory operations
  • Support clinical documentation aligned with research quality standards
  • Contribute to reliable data delivery for research and compliance requirements

Operational Support

  • Resolve routine issues by following established guidelines and processes
  • Work closely with direct supervisors and internal teams
  • Deliver assigned tasks within defined timelines and operational expectations
  • Adapt to rotational work shifts based on project requirements

Required Qualifications

Educational Qualifications

  • Bachelor of Engineering (BE)

Preferred educational backgrounds:

  • Biomedical Engineering
  • Biotechnology
  • Clinical Research
  • Life Sciences
  • Health Informatics
  • Computer Science (if relevant to clinical systems)