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Clinical Data Svs Sr Analyst

2-5 years years
Not Disclosed
10 Aug. 26, 2025
Job Description
Job Type: Full Time Education: Bachelor of Pharmacy/Master of Pharmacy 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

Job Title: Clinical Data Services Senior Analyst

Job No: AIOC-S01600300
Employment Type: Full-time
Experience Required: 2–5 years
Location: Bengaluru, India


About the Role

As a Clinical Data Services Senior Analyst, you will work within Accenture’s Life Sciences R&D vertical, contributing to the execution of critical clinical data management processes. Your role is essential in ensuring high-quality data collection, validation, and delivery for clinical trials that support regulatory submissions and patient safety.

You’ll be responsible for managing and analyzing clinical trial data, leading or contributing to project execution, and interacting with both internal teams and external stakeholders, including clients.


Key Responsibilities

  • Perform advanced clinical data management (CDM) tasks, including:

    • Discrepancy management

    • Query generation and resolution

    • SAE reconciliation

    • Protocol deviation management

  • Create and maintain:

    • CRF Completion Guidelines (CCG)

    • SAE Reconciliation Guidelines

  • Execute edit check validations by:

    • Writing test scripts

    • Creating and executing test cases

    • Performing User Acceptance Testing (UAT) based on CRF/eCRF requirements

  • Support and manage clinical data management projects

  • Ensure data accuracy, consistency, and compliance with regulatory requirements

  • Collaborate with stakeholders including Clinical Research Associates (CRAs), Clinical Research Coordinators (CRCs), and medical monitors


Required Qualifications

  • Education:

    • Bachelor of Pharmacy

    • Master of Pharmacy

  • Experience:

    • 5 to 8 years in clinical data management

    • Practical experience in CRA/CRC roles or medical monitoring is preferred


Desired Skills

  • Strong ability to establish client relationships

  • Capable of managing multiple stakeholders

  • Excellent problem-solving and dispute handling skills

  • Strong team collaboration and deadline management

  • Self-motivated and able to work independently with minimal guidance


Work Environment

  • You will analyze and solve increasingly complex problems

  • Interactions will primarily be with peers, but may also include clients or Accenture management

  • Minimal instruction provided for routine tasks; moderate guidance for new assignments

  • Your decisions may impact your own work and the work of others

  • This is primarily an individual contributor role, but may involve overseeing small teams or work efforts

  • Rotational shift work may be required


About Accenture

Accenture is a global professional services company with leading expertise in digital, cloud, and security. With over 699,000 employees serving clients in more than 120 countries, Accenture offers:

  • Strategy & Consulting

  • Technology

  • Operations

  • Accenture Song

We combine human ingenuity and cutting-edge technology to help clients across 40+ industries transform and grow sustainably.
Visit: www.accenture.com


Important Notes

  • This position may require working in rotational shifts

  • Ensure your qualifications and experience align before applying


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