Apply for IQVIA Hiring Associate Clinical Project Manager Job with global clinical trial and vendor management experience.
IQVIA is hiring experienced professionals for the role of Associate Clinical Project Manager (Trial Vendor Manager) in Thane and Bangalore, India. This opportunity is ideal for candidates with global clinical trial management and vendor oversight experience looking to grow their careers in clinical project management and trial operations.
Candidates with experience in vendor management, global clinical studies, risk management, and operational oversight are encouraged to apply.
Job Details
| Particulars | Details |
|---|---|
| Company Name | IQVIA |
| Job Role | Associate Clinical Project Manager (Trial Vendor Manager) |
| Job Requisition ID | R1546282 |
| Job Locations | Thane, Maharashtra & Bangalore, Karnataka |
| Employment Type | Full-Time |
| Industry | Clinical Research / CRO |
| Experience Required | 3 – 5 Years |
| Qualification | Life Science Background |
| Application Last Date | 30 May 2026 |
About the Company
IQVIA is a leading global provider of clinical research services, healthcare intelligence, and commercial insights for the life sciences industry. The company supports pharmaceutical and healthcare organizations through advanced clinical trial management, analytics, and healthcare technology solutions worldwide.
Job Overview
The Associate Clinical Project Manager is part of the core clinical trial delivery team responsible for project execution, vendor management, operational excellence, and stakeholder coordination.
This role focuses heavily on Trial Vendor Management (TVM) and global clinical trial operations.
Key Responsibilities
Selected candidates will be responsible for:
- Managing vendor relationships in global clinical trials
- Overseeing vendor performance, timelines, quality, and compliance
- Handling vendor-related risk management and issue escalation
- Supporting study start-up activities and vendor specifications
- Managing UAT activities for systems like eCOA and IRT
- Coordinating with Data Management, Medical, Procurement, and Study Leadership teams
- Supporting audit readiness and regulatory compliance
- Handling protocol amendments and vendor reconciliation activities
- Managing multiple vendors across clinical study lifecycles
Vendor Management Experience Required
Candidates should have hands-on experience with:
- IRT
- eCOA
- Central Labs
- Cardiac / ECG Vendors
- PR&R Vendors
- Global vendor oversight and coordination
Required Skills
- Strong stakeholder and communication skills
- Vendor management and negotiation expertise
- Knowledge of GxP and ICH Guidelines
- Risk management and issue resolution skills
- Critical thinking and leadership abilities
- Ability to work independently in global study environments
- Understanding of clinical trial operational processes
Preferred Experience
- Audit and inspection support experience
- Protocol amendment management
- Sponsor/CRO/vendor transition studies
- EU Clinical Trial Regulation (CTR) exposure
- Experience handling multiple vendors simultaneously
Eligibility Criteria
Educational Qualification
- Any Life Science educational background
Experience
- Minimum 3 – 5 years of clinical trial experience as PM / GTM
- Global clinical trial experience is mandatory
- CRA experience alone will not qualify for the PM requirement
- CRA + 2–3 years PM/GTM experience may be considered
Why Join IQVIA?
Working at IQVIA offers:
- Exposure to global clinical trial projects
- Career growth in Clinical Project Management
- International vendor management experience
- Opportunity to work with cross-functional global teams
- Learning opportunities in advanced trial technologies and systems
How to Apply
Interested candidates can apply online through the official career portal of IQVIA before the application deadline.
Important Note
IQVIA follows a strict zero-tolerance policy against candidate fraud. Candidates must provide accurate and truthful information during the hiring process.