IQVIA Recruitment 2026: IQVIA is hiring experienced professionals for TMF Analyst and Senior TMF Analyst positions in India. Candidates with 2–5 years of experience in Trial Master File (TMF) management, clinical documentation, and clinical research can apply for these opportunities.
The job locations include Mumbai, Pune, Noida, and Bangalore. Candidates with experience in electronic Trial Master File (eTMF) systems, Good Clinical Practice (GCP), and clinical trial documentation may be suitable for these roles.
If you are looking for clinical research jobs in India, this opportunity at IQVIA may be worth exploring. Read on for the job details, eligibility criteria, responsibilities, required skills, and application process.
IQVIA Recruitment 2026: Job Overview
| Particulars | Details |
|---|---|
| Company Name | IQVIA |
| Job Role | TMF Analyst / Senior TMF Analyst |
| Job Category | Clinical Research |
| Qualification | Relevant Life Sciences / Pharmacy degree preferred |
| Experience | 2–5 Years |
| Job Location | Mumbai, Pune, Noida, Bangalore |
| Employment Type | Full-Time |
| Industry | Clinical Research / CRO |
| Work Mode | Not specified |
| Eligible Candidates | Experienced Professionals |
| Application Mode | |
| Email Address | priyanka.tyagi2@quintiles.com |
Note: The recruitment information provided specifies 2–5 years of relevant experience. Freshers are not eligible for these particular positions.
About IQVIA
IQVIA is a global provider of clinical research services, healthcare analytics, and technology solutions. The company works with pharmaceutical, biotechnology, and medical device organizations to support clinical development and healthcare innovation.
IQVIA provides clinical trial management and related services, helping organizations manage clinical research projects and meet regulatory requirements.
Working as a TMF Analyst at IQVIA offers experienced professionals an opportunity to work with clinical operations teams and contribute to clinical trial documentation and compliance activities.
Job Positions at IQVIA
IQVIA is recruiting for the following positions:
- TMF Analyst
- Senior TMF Analyst
Candidates with relevant experience in clinical trial documentation, eTMF systems, and document quality management can consider applying.
Job Locations
The openings mentioned are available in the following Indian cities:
- Mumbai, Maharashtra
- Pune, Maharashtra
- Noida, Uttar Pradesh
- Bangalore, Karnataka
Candidates interested in these locations can contact the recruiter to confirm the availability of their preferred location.
Eligibility Criteria
Candidates interested in IQVIA TMF Analyst recruitment should meet the following requirements.
Educational Qualification
Graduates in relevant life sciences or pharmacy disciplines may be suitable for these positions. Applicants should check the specific educational requirements with the recruiter.
Work Experience
- 2–5 years of relevant professional experience.
- Experience in TMF management or clinical trial documentation.
- Familiarity with electronic Trial Master File systems.
- Experience maintaining clinical research records.
Freshers without relevant professional experience are not eligible for the roles described in this recruitment announcement.
Key Responsibilities of a TMF Analyst
Selected candidates may be responsible for the following activities.
1. Clinical Trial Documentation Management
- Manage clinical trial documentation and maintain accurate records.
- Upload, review, organize, and archive essential clinical trial documents.
- Ensure documents are filed according to applicable TMF requirements.
- Maintain the completeness and accuracy of clinical trial records.
2. Trial Master File Management
- Support day-to-day TMF activities across clinical research projects.
- Perform document quality reviews and completeness checks.
- Identify missing documents and follow up on outstanding documentation.
- Help maintain inspection-ready Trial Master Files.
3. Regulatory Compliance
- Follow company Standard Operating Procedures (SOPs).
- Ensure documentation complies with applicable Good Clinical Practice (GCP) requirements.
- Follow sponsor-specific documentation guidelines.
- Support audit and inspection readiness activities.
4. Project Team Coordination
- Coordinate with clinical operations and project management teams.
- Support clinical trial teams with documentation-related queries.
- Track document discrepancies and assist with their resolution.
- Complete assigned activities within project timelines.
Required Skills for TMF Analyst Jobs
Candidates applying for these positions should have relevant technical knowledge and professional skills.
- Knowledge of Trial Master File management.
- Understanding of ICH-GCP guidelines.
- Experience with eTMF platforms such as Veeva Vault TMF, Phlexglobal, or Trial Interactive.
- Knowledge of clinical trial documentation and essential records.
- Strong attention to detail.
- Good written and verbal communication skills.
- Ability to work with international clinical research teams.
- Understanding of document quality control and inspection readiness.
Experience with specific eTMF platforms may vary according to the position and project requirements.
What Is a Trial Master File (TMF)?
A Trial Master File is a collection of essential documents that demonstrate how a clinical trial has been conducted and managed.
These documents help establish that a clinical trial complies with applicable regulations, ethical requirements, and Good Clinical Practice guidelines.
TMF Analysts play an important role in maintaining these records, ensuring that documents are accurate, complete, organized, and accessible when required for audits or regulatory inspections.
Professionals working in TMF management may use electronic systems to organize and track clinical trial documents throughout the study lifecycle.
How to Apply for IQVIA Recruitment 2026?
Interested and eligible candidates can apply by sending their updated resumes to the recruitment email address provided in the job announcement.
Recruitment Email: priyanka.tyagi2@quintiles.com
Udemy Affiliate Link: https://trk.udemy.com/E0PXVe
Course: Certification in Drug Regulatory Affairs – Medical Devices
Suggested Email Subject:
Application for TMF Analyst / Senior TMF Analyst – Your Name – Your Experience
Before applying, make sure your resume highlights your relevant experience in TMF management, clinical documentation, eTMF platforms, and GCP compliance.
Candidates should verify the current availability of the position and the recruitment contact before sharing personal information.
Why Consider a Career in TMF Management?
TMF management is an important function within clinical research. Professionals in this field work with clinical operations teams to maintain essential study documentation and support regulatory compliance.
With experience in eTMF platforms, document quality control, and clinical trial processes, professionals may explore opportunities in TMF management, clinical operations, and related documentation roles.
The skills developed in TMF management can also be relevant to other positions involving clinical trial documentation and quality processes.
Frequently Asked Questions (FAQs)
1. Is IQVIA hiring TMF Analysts in 2026?
According to the recruitment information provided, IQVIA is hiring for TMF Analyst and Senior TMF Analyst positions in India. Candidates should confirm whether the vacancies are still open before applying.
2. What is the required experience for IQVIA TMF Analyst jobs?
The stated experience requirement is 2–5 years in TMF management, clinical documentation, or a related field.
3. Are freshers eligible for IQVIA TMF Analyst recruitment?
No. The openings described are intended for experienced professionals. Freshers are not eligible.
4. What are the job locations for IQVIA TMF Analyst vacancies?
The locations mentioned are Mumbai, Pune, Noida, and Bangalore.
5. How can I apply for IQVIA TMF Analyst jobs?
You can send your updated resume to priyanka.tyagi2@quintiles.com, using a clear subject line mentioning the position and your experience.
6. What skills are required for a TMF Analyst position?
Relevant skills include TMF management, eTMF systems, ICH-GCP knowledge, clinical trial documentation, document quality control, and communication.
7. Is this a work-from-home job?
The work mode has not been confirmed in the supplied recruitment information. Candidates should contact the recruiter to check whether remote or hybrid work is available.
Final Words
IQVIA’s TMF Analyst and Senior TMF Analyst recruitment may be relevant for experienced clinical research professionals looking to develop their careers in Trial Master File management.
Candidates with 2–5 years of relevant experience, knowledge of GCP, and familiarity with eTMF systems can review the requirements and contact the recruiter for further details.
If you meet the eligibility criteria, prepare your updated resume and apply using the email address provided above. Make sure to verify the vacancy status before submitting your application.