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Clinical Data Svs Associate

Accenture
Accenture
0-3 years
Not Disclosed
Bengaluru, India
10 March 12, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Clinical Data Services Associate

Company: Accenture
Location: Bengaluru, India
Job Type: Full-Time
Job ID: AIOC-S01630114
Industry: Life Sciences / Clinical Research / Clinical Data Management

Experience Required: 0–2 Years (Typically 1–3 Years Preferred)
Education: BE or MSc in a relevant discipline

About Accenture
Accenture is a leading global professional services company with strong expertise in digital transformation, cloud computing, and cybersecurity solutions. With more than 784,000 employees serving clients in over 120 countries, Accenture delivers innovative services across Strategy and Consulting, Technology, Operations, and Accenture Song.

Within the Life Sciences sector, Accenture supports pharmaceutical and biotechnology companies across the entire research and development lifecycle, including clinical research support, pharmacovigilance, regulatory services, and patient engagement solutions. The organization helps global healthcare companies accelerate innovation and improve patient outcomes by combining scientific knowledge with advanced technologies and analytics.

Job Overview
Accenture is seeking a Clinical Data Services Associate to join its Life Sciences R&D team in Bengaluru. This role focuses on clinical data management activities that support the collection, validation, and analysis of clinical trial data.

The selected candidate will contribute to ensuring the accuracy, integrity, and regulatory compliance of data generated during clinical research studies. This position provides an excellent opportunity for early-career professionals interested in building expertise in clinical data management, electronic data capture systems, and clinical trial data processes.

Key Responsibilities

  • Support clinical data management processes including data collection, validation, and quality review for clinical trials.

  • Assist in building and testing clinical databases and electronic data capture (EDC) systems used in clinical research studies.

  • Perform clinical database programming and testing to ensure system functionality and data accuracy.

  • Validate and review clinical data to ensure compliance with clinical research protocols and regulatory requirements.

  • Maintain accurate documentation and audit-ready records related to clinical data management activities.

  • Collaborate with clinical research teams to resolve data queries and ensure data consistency.

  • Contribute to maintaining high-quality datasets for regulatory submissions and clinical study analysis.

Required Skills and Competencies

  • Basic understanding of clinical research and clinical data management processes.

  • Knowledge of clinical database programming, testing, and Electronic Data Capture (EDC) systems.

  • Strong analytical and problem-solving skills with attention to data accuracy.

  • Ability to manage multiple stakeholders and collaborate within cross-functional teams.

  • Good communication skills and the ability to maintain strong client relationships.

  • Capability to handle task coordination and resolve operational issues effectively.

Roles and Responsibilities

  • Perform routine clinical data management tasks following standard guidelines and procedures.

  • Work closely with the immediate team and report to the direct supervisor for guidance and task coordination.

  • Execute daily work assignments with moderate to detailed instructions depending on task complexity.

  • Contribute as an individual team member within a defined scope of clinical data management activities.

  • Ensure all assigned tasks meet quality standards and are completed within defined timelines.

  • Be flexible to work in rotational shifts based on project and client requirements.

Why Join This Role
This role offers a strong foundation for professionals seeking careers in clinical research, clinical data management, and pharmaceutical research operations. Candidates will gain exposure to clinical trial data workflows, regulatory standards, and advanced clinical research technologies used by global pharmaceutical companies.

Job Location
Bengaluru, India.