Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Data Svs Sr Analyst

Accenture
Accenture
2-5 years
Not Disclosed
Mumbai, India
10 April 21, 2026
Job Description
Job Type: Full Time Education: B.sc/ M.sc/ B.Pharm/ M.Pharm/ Life Science 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

Job Title

Clinical Data Services – Senior Analyst

Company

Accenture

Location

Mumbai, India

Experience

5–8 years

Qualification

Master of Science (MSc)


Job Summary

The Clinical Data Services Senior Analyst will be part of the Life Sciences R&D team, responsible for managing clinical trial data to ensure accuracy, integrity, and compliance with regulatory standards. The role involves end-to-end clinical data management, supporting study conduct and enabling high-quality data for analysis of safety and efficacy of medical treatments.


Key Responsibilities

  • Perform end-to-end clinical data management activities

  • Ensure accurate data collection, validation, and cleaning

  • Review and resolve data discrepancies

  • Maintain data quality and compliance with regulatory requirements

  • Work with Electronic Data Capture (EDC) systems (e.g., Medidata Rave)

  • Support study setup, execution, and database lock activities

  • Collaborate with cross-functional teams and stakeholders

  • Deliver projects within timelines and quality standards

  • Maintain documentation as per industry guidelines


Required Skills & Competencies

Technical Skills

  • Strong understanding of:

    • Clinical trial processes

    • Clinical Data Management (CDM)

    • Regulatory guidelines (ICH-GCP)

  • Experience with:

    • EDC platforms (preferably Medidata Rave)

  • Knowledge of data validation and discrepancy management

Soft Skills

  • Attention to detail and accuracy

  • Strong analytical and problem-solving skills

  • Effective communication skills

  • Ability to work under pressure

  • Adaptability and flexibility

  • Strong client relationship management


Experience Requirements

  • 2–5 years of relevant experience in Clinical Data Management

  • Exposure to Medidata Rave EDC platform preferred


Business Unit

Life Sciences R&D


Functional Area

Clinical / Pharmacovigilance / Regulatory Services


Key Objectives

  • Ensure high-quality clinical data for analysis

  • Support regulatory compliance

  • Enable successful clinical trial outcomes

  • Contribute to patient safety and drug development


Work Environment

  • Collaborative and inclusive workplace

  • Opportunities for continuous learning and certification

  • Exposure to global clients and projects


Equal Employment Opportunity

Accenture is an equal opportunity employer. All employment decisions are made without discrimination based on legally protected characteristics.


Important Notice

  • Accenture does not charge any fees during the hiring process

  • Candidates should report any fraudulent recruitment communication