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Clinical Data Services Associate Job in Mumbai at Accenture

Accenture hiring Clinical Data Services Associate in Mumbai. Apply for eTMF and clinical data management role with B.Pharm experience required.


Introduction

Candidates with experience in clinical data management and documentation have a strong opportunity in the healthcare consulting domain. Accenture is hiring for the role of Clinical Data Services Associate in Mumbai. This role is ideal for pharmacy graduates with experience in eTMF management and clinical trial documentation.


Company Overview

Accenture is a leading global professional services organization specializing in digital, cloud, and operations. With a strong presence in healthcare and life sciences, Accenture supports pharmaceutical companies through clinical, regulatory, and pharmacovigilance services.


Job Location & Employment Type

  • Location: Mumbai, Maharashtra, India
  • Job Type: Full-Time
  • Industry: Clinical Data Management / eTMF / Life Sciences

Job Overview (Job Details Table)

Job TitleClinical Data Services Associate
Company NameAccenture
QualificationBachelor of Pharmacy (B.Pharm)
Experience2 – 4 Years
Job LocationMumbai, Maharashtra
Employment TypeFull-Time
SalaryAs per company norms
Application ModeOnline Application
DepartmentClinical Data Services / eTMF
Job IDAIOC-S01612907

Open Positions / Department Details

The role is part of the Life Sciences R&D and Clinical Data Management Team, focusing on clinical trial documentation, eTMF management, and regulatory submission support.


Key Roles & Responsibilities

As a Clinical Data Services Associate, your responsibilities will include:

Clinical Data Management

  • Performing data management activities such as:
    • Discrepancy review
    • Query generation and resolution
  • Supporting database validation (UAT) and edit checks
  • Assisting in CRF (Case Report Form) completion guidelines

eTMF & Document Management

  • Managing Trial Master File (TMF) and clinical documentation
  • Performing format checks for eCTD submissions
  • Ensuring compliance with:
    • Good Documentation Practices (GDP)
    • eCTD standards
  • Conducting:
    • PDF property checks
    • Bookmark and hyperlink validation
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Study & Project Support

  • Supporting clinical trial documentation lifecycle
  • Reviewing:
    • Protocol packages
    • Study checklists
    • Clinical study report appendices
  • Performing document reconciliation and quality checks
  • Coordinating with internal teams and clients

Eligibility Criteria

Educational Qualification

  • Bachelor of Pharmacy (B.Pharm)

Experience Required

  • 2 to 4 years of experience in:
    • Clinical data management
    • eTMF/document management
    • Regulatory or clinical operations

Skills Required

  • Knowledge of:
    • Clinical Data Management processes
    • eTMF and eCTD requirements
  • Understanding of:
    • Clinical trial lifecycle
    • Regulatory documentation
  • Strong attention to detail and documentation skills
  • Ability to work under pressure and meet deadlines
  • Problem-solving and analytical skills
  • Good communication and client interaction skills

Salary & Benefits

  • Salary: As per company norms
  • Opportunity to work with a global consulting leader
  • Exposure to end-to-end clinical trial processes
  • Career growth in clinical data and regulatory domains
  • Collaborative and technology-driven work environment

Selection Process

The recruitment process may include:

  1. Application Screening
  2. Technical/Functional Interview
  3. Assessment (if required)
  4. HR Discussion
  5. Final Selection

How to Apply

Interested candidates should apply through the official Accenture careers portal.

Ensure your resume highlights:

  • Clinical data management experience
  • eTMF/eCTD knowledge
  • Regulatory documentation exposure

Important Dates

  • Application Deadline: Not specified (apply as soon as possible)

Why Apply for This Pharma Job?

This role is ideal for candidates aiming to grow in clinical data and regulatory domains:

  • Work with a global leader (Accenture)
  • Gain expertise in eTMF and clinical documentation systems
  • Exposure to global clinical trial processes
  • Opportunity to work on regulatory submissions
  • Strong career path in life sciences consulting

Important Note / Disclaimer

IndiaPharmaJobs.in is an independent job information platform and is not affiliated with any recruiter or company. Candidates are advised to verify all details independently before applying. We do not charge any fee for job applications.

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Final Call-to-Action

If you have experience in clinical data management and documentation, apply at the earliest. This Accenture opportunity can help you build a strong career in clinical operations and regulatory services.

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