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Clinical Data Svs Sr Analyst

Accenture
Accenture
5-8 years
preferred by company
10 Jan. 2, 2026
Job Description
Job Type: Full Time Hybrid 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 Senior Analyst

Job ID: AIOC-S01619739
Company: Accenture
Location: Bengaluru, India
Employment Type: Full-Time
Work Mode: Hybrid / Office-based
Functional Area: Clinical Data Management / Clinical Data Operations
Experience Required: 5–8 years
Education Requirement: BE / BTech


About Accenture

Accenture is a global professional services leader with unmatched capabilities across digital, cloud, security, and intelligent operations. Serving clients in more than 120 countries, Accenture combines deep industry expertise with advanced technology to help organizations drive innovation, efficiency, and measurable outcomes. Within the Life Sciences R&D vertical, Accenture supports leading biopharmaceutical companies across clinical development, pharmacovigilance, regulatory affairs, and patient services.


Role Overview

The Clinical Data Services Senior Analyst will support end-to-end clinical data operations with a strong focus on clinical database testing and validation. This role plays a critical part in ensuring the accuracy, integrity, and regulatory compliance of clinical trial data, enabling high-quality data delivery for safety and efficacy evaluations. The position is ideal for professionals with hands-on experience in EDC systems, UAT testing, and clinical data management processes.


Key Responsibilities

  • Design, test, and validate Electronic Data Capture (EDC) databases in accordance with clinical trial protocols and regulatory standards.

  • Develop and execute User Acceptance Testing (UAT) plans, including test scripts, test cases, and documentation.

  • Verify database requirements for eCRFs, edit checks, data extractions, listings, and reports.

  • Support clinical external data loading and reconciliation activities.

  • Ensure clinical data accuracy, consistency, and compliance throughout the trial lifecycle.

  • Analyze and resolve complex data-related issues with minimal supervision.

  • Collaborate with internal teams, stakeholders, and client representatives to support clinical trial deliverables.

  • Contribute as an individual contributor and, where required, oversee small workstreams or junior team members.

  • Adhere to project timelines, quality standards, and regulatory requirements.

  • Participate in rotational shifts as per project needs.


Required Skills & Expertise

  • Clinical Database Testing

  • Clinical Data Operations and Management

  • External Data Loading and Reconciliation

  • EDC systems and UAT processes

  • Strong analytical, problem-solving, and documentation skills

  • Ability to work independently in a fast-paced, regulated environment


Experience & Qualifications

  • 5 to 8 years of relevant experience in clinical data management or clinical data operations.

  • Proven experience in clinical database testing and UAT activities.

  • Bachelor’s degree in Engineering (BE/BTech) or a related technical discipline.


Why Join Accenture Life Sciences R&D?

This role offers exposure to global clinical research programs, advanced data platforms, and cross-functional collaboration within the life sciences domain. You will contribute to high-impact clinical trials while working with cutting-edge technologies and industry-leading processes.