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Clinical Data Svs Sr Analyst

2-5 years
Not Disclosed
10 Dec. 2, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Location: Bengaluru, India
Job Type: Full Time
Experience Required: 2–5 years (overall), 5–8 years preferred in Clinical Data Services
Job ID: AIOC-S01615157

Position Overview

Accenture is seeking a Clinical Data Services Senior Analyst to support its Life Sciences R&D vertical. The role focuses on end-to-end clinical data management, SDTM mapping, data integration, and quality review to ensure accurate delivery of clinical trial data aligned with global CDISC standards.

This position is ideal for professionals experienced in SDTM Mapping, Clinical Data Management, and Life Sciences Data Operations.


Key Responsibilities

  • Perform comprehensive review and analysis of raw clinical data.

  • Develop and author mapping specifications from source data to CDISC/SDTM standards or client-defined formats.

  • Create SDTM domains using data conversion tools and ensure high-quality output through QC processes.

  • Prepare data definition files and annotate CRFs according to CDISC/SDTM guidelines.

  • Conduct discrepancy management, query generation and resolution, edit check testing, and UAT support.

  • Identify protocol deviations, create test cases and test scripts, and validate clinical databases.

  • Support end-to-end clinical data management projects, documentation, and status reporting.

  • Proactively recognize data issues and contribute to solutions to maintain deliverable quality.

  • Collaborate with cross-functional teams within Clinical, Pharmacovigilance, and Regulatory services.

  • Work with limited supervision on daily tasks and moderate guidance for new assignments.

  • May work in rotational shifts as required.


Required Skills and Competencies

  • Strong understanding of CDISC, SDTM standards, CRF design, UAT, and clinical database structures.

  • Analytical and problem-solving mindset with high attention to detail.

  • Ability to work under pressure while ensuring consistent quality.

  • Adaptability, quick learning capability, and strong execution skills.

  • Ability to function as an individual contributor or manage small work efforts.


Education & Experience

  • Qualifications: BE/BTech

  • Experience:

    • Minimum: 2–5 years in Clinical Data Services

    • Preferred: 5–8 years with hands-on experience in SDTM mapping and clinical data operations


About Accenture

Accenture is a global professional services leader delivering strategy, consulting, technology, and operations solutions across 120+ countries. With extensive expertise across more than 40 industries, Accenture enables clients to harness technology and human ingenuity to drive innovation and sustained growth.

The Life Sciences R&D vertical supports pharmaceutical and biotechnology organizations across clinical trials, regulatory operations, pharmacovigilance, and patient services. Accenture promotes a culture of inclusion, continuous learning, and high-impact work experiences for all employees.


Equal Employment Opportunity

Accenture maintains a strict non-discrimination policy across all employment decisions including hiring, compensation, promotions, and training. All applicants are considered without regard to age, gender, race, disability, nationality, or any protected category.


Important Notice

Accenture does not charge any fees at any stage of recruitment. If you receive communication asking for payment, contact india.fc.check@accenture.com immediately.