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 Title | Clinical Data Services Associate |
|---|---|
| Company Name | Accenture |
| Qualification | Bachelor of Pharmacy (B.Pharm) |
| Experience | 2 – 4 Years |
| Job Location | Mumbai, Maharashtra |
| Employment Type | Full-Time |
| Salary | As per company norms |
| Application Mode | Online Application |
| Department | Clinical Data Services / eTMF |
| Job ID | AIOC-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
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:
- Application Screening
- Technical/Functional Interview
- Assessment (if required)
- HR Discussion
- 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.
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.