IQVIA is inviting applications for the Sr CD Project Support Assistant position in Thane, Maharashtra. This is an excellent opportunity for candidates with experience in clinical research operations, project coordination, Trial Master File (TMF) management, clinical documentation, and project support to join one of the world’s leading clinical research organizations.
If you are looking to build a career in Clinical Project Management, Clinical Operations, Clinical Trial Administration, or Clinical Research Support, this IQVIA job offers exposure to global clinical trials while working alongside experienced project managers and cross-functional teams.
Job Details
| Particular | Details |
|---|---|
| Job Title | Sr CD Project Support Assistant |
| Company | IQVIA |
| Location | Thane, Maharashtra, India |
| Job Type | Full-Time |
| Department | Clinical Development |
| Experience | Minimum 1 Year |
| Application Deadline | 4 August 2026 |
Key Responsibilities
The selected candidate will support Project Managers throughout the clinical study lifecycle by performing activities such as:
- Prepare and maintain study trackers.
- Update sponsors with project progress.
- Support preparation of clinical study documentation.
- Manage Connected Devices application and database access requests.
- Coordinate document translations with external vendors.
- Perform periodic access reviews for project systems.
- Create, organize, and maintain the Trial Master File (TMF).
- Upload project documents into logistics systems.
- Coordinate with logistics teams for site creation and updates.
- Support project archival activities.
- Train and mentor junior Project Support Assistants when required.
- Maintain project metrics and customer satisfaction surveys.
- Coordinate vendor communication and analyze vendor costs.
- Maintain vendor files and proposal documentation.
Required Qualifications
Applicants should possess:
- High School Diploma or equivalent qualification (preferred).
- Minimum 1 year of relevant experience in clinical research or project support.
- Strong knowledge of Microsoft Excel and Microsoft Word.
- Good organizational and documentation skills.
- Ability to communicate effectively with internal teams, vendors, and clients.
- Strong attention to detail and time management.
Preferred Skills
- Clinical Project Support
- Trial Master File (TMF)
- Clinical Documentation
- Clinical Operations
- Vendor Coordination
- Logistics Coordination
- Microsoft Excel
- Microsoft Word
- Project Tracking
- Study Documentation
- Clinical Trial Administration
- Team Collaboration
Salary
Based on similar IQVIA Clinical Project Support roles in India, the estimated salary is:
โน4.8 LPA โ โน7.8 LPA
(Actual salary depends on experience, skills, and company policies.)
Why Join IQVIA?
Working at IQVIA provides numerous career advantages:
- Global clinical research exposure
- Opportunity to work on international clinical studies
- Excellent learning and career growth
- Exposure to Clinical Operations and Project Management
- Collaborative work environment
- Professional development opportunities
- Competitive compensation and employee benefits
Who Should Apply?
This opportunity is suitable for candidates with backgrounds in:
- B.Pharm
- M.Pharm
- Pharm.D
- B.Sc Life Sciences
- M.Sc Life Sciences
- Biotechnology
- Clinical Research
- Healthcare Sciences
- Candidates with relevant clinical project support experience
How to Apply
