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Clinical Data Services Associate

Accenture
Accenture
0-3 years
preferred by company
Bangalore, India
1 May 18, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Clinical Data Services Associate

Location: Bengaluru, India
Job Type: Full-Time
Work Mode: Onsite / Rotational Shifts
Industry: Clinical Research | Clinical Data Management | Life Sciences | Healthcare
Department: Clinical Data Services
Experience Required: 0–3 Years (Freshers Eligible for Entry-Level Roles)
Qualification Required: B.E / M.Sc
Job Reference ID: AIOC-S01645852
Employment Type: Individual Contributor

Job Overview

A leading global professional services organization is hiring a Clinical Data Services Associate for its Bengaluru location. This opportunity is ideal for candidates interested in building a career in clinical research, clinical data management, clinical database testing, and electronic data capture (EDC) systems.

The selected candidate will support clinical trial data management operations, ensuring accurate collection, validation, management, and quality control of clinical research data to support pharmaceutical and life sciences studies.

This is an excellent opportunity for freshers and early-career professionals looking to establish themselves in clinical data management and life sciences operations.

Key Responsibilities

Clinical Data Management

  • Support clinical data management activities for ongoing clinical trials and research programs.
  • Ensure accurate collection, review, validation, and maintenance of clinical trial data.
  • Assist in maintaining data quality, completeness, consistency, and regulatory compliance.

Clinical Database Operations

  • Support clinical database testing activities.
  • Assist in validation and quality review of clinical databases used for trial data management.
  • Help ensure databases function accurately according to study and operational requirements.

Clinical EDC Build Support

  • Support Electronic Data Capture (EDC) build and configuration activities.
  • Assist in study database setup, testing, and maintenance.
  • Help ensure proper functioning of data capture systems used in clinical studies.

Clinical Research Data Processing

  • Process and manage data collected during clinical trials.
  • Support integration, storage, and quality review of research data.
  • Assist in preparing high-quality clinical datasets for downstream analysis.

Quality & Regulatory Compliance

  • Follow clinical research data management procedures, quality standards, and compliance requirements.
  • Ensure data handling aligns with regulatory expectations and organizational guidelines.
  • Support audit-ready documentation and data traceability practices.

Team Collaboration

  • Work closely with internal teams and reporting managers.
  • Support assigned operational tasks as an individual contributor.
  • Resolve routine operational issues based on standard procedures and guidance.

Operational Requirements

  • Manage day-to-day assigned clinical data operations tasks.
  • Adapt to rotational shift schedules based on business requirements.
  • Maintain productivity and quality expectations for assigned deliverables.

Educational Qualification

Candidates must have:

  • B.E (Bachelor of Engineering)
    OR
  • M.Sc (Master of Science)

Preferred educational backgrounds:

  • Life Sciences
  • Biotechnology
  • Biomedical Sciences
  • Bioinformatics
  • Clinical Research
  • Computer Science (for EDC/database support roles)

Experience Requirements

  • 0–3 years of experience in clinical data management, clinical operations, or healthcare data roles
  • Freshers may apply for entry-level opportunities
  • Prior exposure to clinical research data systems will be an advantage