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Clinical Data Svs Sr Analyst

Accenture
2-5 years
INR 7 LPA – 12 LPA
Mumbai, India
1 June 12, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Communication Skills, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing

Clinical Data Services Senior Analyst

Company: Accenture
Job ID: AIOC-S01649818
Location: Mumbai
Employment Type: Full Time
Department: Clinical Data Services – Clinical Data Management
Qualification: Bachelor of Pharmacy (B.Pharm)
Experience: 2–5 years (Role requirements) | 5–8 years (Designation level mentioned)


About the Role

Accenture is hiring a Clinical Data Services Senior Analyst to support Clinical Data Management activities within its Life Sciences R&D practice. The role focuses on ensuring accurate, high-quality clinical trial data collection, validation, integration, and management while maintaining compliance with regulatory standards and industry best practices.

The selected candidate will work closely with global clinical research teams, helping pharmaceutical and biotechnology clients improve clinical trial outcomes through efficient data management processes.


Key Responsibilities

  • Manage and support Clinical Data Management (CDM) activities across clinical studies.
  • Ensure clinical trial data is collected, validated, reviewed, and maintained accurately.
  • Work with Electronic Data Capture (EDC) platforms, preferably Medidata RAVE.
  • Perform data cleaning, discrepancy management, and query resolution activities.
  • Ensure compliance with clinical trial regulations, GCP guidelines, and internal SOPs.
  • Collaborate with cross-functional stakeholders including Clinical Operations, Biostatistics, and Regulatory teams.
  • Support study database reviews and data quality checks.
  • Deliver quality data management outputs within project timelines.
  • Participate in client interactions and stakeholder discussions.
  • Maintain accurate study documentation and audit readiness.

Required Skills

  • Clinical Data Management (CDM)
  • Clinical Trial Process Knowledge
  • Medidata RAVE EDC (Preferred)
  • Data Validation & Data Cleaning
  • Query Management
  • Regulatory Compliance & GCP
  • Stakeholder Management
  • Strong Communication Skills
  • Attention to Detail
  • Ability to Manage Multiple Priorities

Preferred Experience

  • 2–5 years of Clinical Data Management experience.
  • Experience working on global clinical trials.
  • Exposure to Medidata RAVE or similar EDC systems.
  • Understanding of clinical research regulations and guidelines.
  • Experience handling multiple studies simultaneously.

Ideal Candidate Profile

  • B.Pharm graduate with relevant Clinical Data Management experience.
  • Strong analytical and organizational skills.
  • Comfortable working with global stakeholders and tight timelines.
  • Detail-oriented professional with a focus on data quality and compliance.