Apply online for IQVIA pharma jobs for freshers and experienced candidates with TMF analyst role eligibility, salary and application details.
Introduction
If you are aiming to build a career in clinical research documentation and trial management, this opportunity at IQVIA is worth exploring. The company is hiring for the Sr TMF Analyst role across multiple locations in India. This position is ideal for professionals with experience in Trial Master File (TMF) management, records handling, and clinical research compliance.
Job Overview
| Details | Information |
|---|---|
| Job Title | Sr TMF Analyst |
| Company Name | IQVIA |
| Location | Thane, Bangalore, Pune |
| Employment Type | Full-Time |
| Department | Clinical Research / Records Management |
| Experience Required | Minimum 4 Years |
| Education | Bachelor’s Degree (Records Management or related field) |
| Salary | As per company norms |
Company Overview
IQVIA is a global leader in clinical research services, healthcare analytics, and commercial insights. The company works with pharmaceutical and biotech organizations worldwide to accelerate drug development and improve patient outcomes. With advanced technology and data-driven solutions, IQVIA plays a key role in shaping the future of healthcare.
Job Location & Employment Type
- Locations:
- Thane, Maharashtra
- Bangalore, Karnataka
- Pune, Maharashtra
- Employment Type: Full-Time
This is a multi-location role offering flexibility to work from major clinical research hubs in India.
Open Positions / Department Details
- Role: Senior TMF Analyst
- Department: Clinical Research / Records Management
- Function: Trial Master File (TMF) and Records Management
The position focuses on managing clinical trial documentation and ensuring compliance with global regulatory standards.
Key Roles & Responsibilities
The Sr TMF Analyst IQVIA role includes the following responsibilities:
- Act as a liaison between Records Management and project teams
- Manage Trial Master Files (TMF) across multiple projects and sites
- Ensure compliance with SOPs, GCP guidelines, and regulatory requirements
- Coordinate transfer, storage, retrieval, and disposal of clinical records
- Monitor filing accuracy and ensure adherence to file plans
- Handle imaging and scanning processes for clinical documents
- Train team members on records management procedures
- Maintain data integrity and security of records
- Support internal and external stakeholders with documentation needs
- Prepare closed studies for archiving within timelines
- Oversee storage space and ensure proper document handling
- Assist management in planning and executing records management strategies
- Lead or support teams in TMF-related projects
Eligibility Criteria
Education
- Bachelor’s degree in Records Management or related field
Experience
- Minimum 4 years of experience in records management or clinical research
- Experience in TMF handling is highly preferred
Skills Required
- Strong knowledge of ICH guidelines and Good Clinical Practice (GCP)
- Understanding of regulatory requirements in clinical research
- Experience with records management systems and tools
- Excellent organizational and multitasking abilities
- Strong communication and documentation skills
- Ability to analyze problems and make effective decisions
- Leadership and team coordination skills
Salary & Benefits
- Salary: As per company norms
Additional benefits may include:
- Health and wellness programs
- Career growth opportunities in clinical research
- Exposure to global clinical trials
- Learning and development support
Selection Process
The recruitment process generally includes:
- Online application submission
- Resume screening
- Technical interview (TMF / Clinical Research focus)
- HR discussion
- Final selection
How to Apply
Interested candidates can apply through the official IQVIA careers portal. Ensure your resume highlights your experience in TMF management, regulatory compliance, and clinical documentation.
Important Dates
- Last Date to Apply: May 9, 2026
Why Apply for This Job?
The Sr TMF Analyst IQVIA Jobs 2026 role offers excellent career growth in clinical research and documentation management. Here’s why this job stands out:
- Work with a globally recognized clinical research organization
- Gain exposure to international clinical trial standards
- Opportunity to handle large-scale research documentation
- Strong career progression in TMF and clinical operations
- Enhance your expertise in regulatory compliance and GCP
This role is especially valuable for professionals seeking clinical research jobs in India and aiming to specialize in Trial Master File management.
FAQs
1. What is the role of a Sr TMF Analyst at IQVIA?
The role involves managing clinical trial documents, ensuring compliance, and handling Trial Master Files.
2. What experience is required for this job?
A minimum of 4 years of experience in records management or clinical research is required.
3. Is this job available in multiple locations?
Yes, the role is available in Thane, Bangalore, and Pune.
4. What qualifications are required?
A bachelor’s degree in records management or a related field is required.
5. How can I apply for this job?
You can apply online through the official IQVIA careers website.
Conclusion
The Sr TMF Analyst IQVIA Jobs 2026 opportunity is ideal for experienced professionals in clinical research and records management. With global exposure, structured processes, and strong career growth, this role can significantly enhance your professional journey. Apply now to take the next step in your career.
Disclaimer
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