Syneos Health Hiring TMF Specialist I - Hyderabad
Are you seeking high-paying Syneos Health Careers India or TMF Specialist Jobs Hyderabad? Globally leading Contract Research Organization (CRO) Syneos Health has announced recruitment for a **TMF Specialist I** based at its Hyderabad office. This is a full-time, hybrid position open to candidates with 1 or more years of experience.
Selected candidates will manage Trial Master File (TMF) setups, conduct document indexing and quality reviews, perform completeness reviews against expected lists, and collaborate with global clinical operations. To prepare your application details, check out our guide on how to apply for healthcare and pharma jobs online.
📋 Job Details
| Particulars | Details |
|---|---|
| Position | TMF Specialist I |
| Company | Syneos Health |
| Location | Hyderabad, Telangana, India (Hybrid) |
| Work Mode | Hybrid (Office-based) |
| Employment Type | Full-Time |
| Experience Required | 1+ Years |
| Qualifications | B.Sc, M.Sc, B.Pharm, M.Pharm, BDS |
| Department | Trial Master File (TMF) Operations |
| Job ID | 25109887 |
| Salary Package | Competitive (Based on experience) |
| Application Deadline | July 3, 2026 |
💼 Key Responsibilities
- Support Trial Master File (TMF) setup, maintenance, and study close-out activities throughout the clinical trial lifecycle.
- Process clinical study documentation in complete compliance with SOPs, ICH-GCP guidelines, and regulatory requirements.
- Scan, index, upload, and file clinical documents into electronic Trial Master File (eTMF) systems.
- Perform detailed Quality Reviews of documents submitted by study teams to check for legibility and attributes compliance.
- Conduct Completeness Reviews against study Expected Document Lists.
- Maintain secure and accurate documentation for active and archived clinical studies.
- Ensure continuous inspection readiness for internal audits and external regulatory inspections.
- Collaborate actively with global clinical operations and project managers.
Reviewing and quality-checking essential document logs require a clear understanding of GCP guidelines. To check your compliance knowledge, try our interactive Clinical Trial Assistant (CTA) Quiz.
🎓 Qualifications & Experience Requirements
Candidates applying for this specialist position should meet the following:
- Education: Bachelor’s or Master’s degree in Life Sciences, Pharmacy, BDS, or related scientific disciplines.
- Eligible Degrees: B.Sc, M.Sc, B.Pharm, M.Pharm, BDS.
- Experience: Minimum 1 year of experience in Trial Master File (TMF), Electronic TMF (eTMF), or as a Clinical Research Coordinator (CRC) managing site files.
For pharmacy graduates interested in international careers vs national roles, read our salary and career guide on B.Pharm Careers: India vs USA.
Required Core Skills
- Knowledge of ICH-GCP guidelines and clinical trial regulations.
- Familiarity with medical terminology and clinical documentation types.
- Hands-on experience using eTMF platforms.
- Proficiency in Microsoft Office applications and Adobe Acrobat.
- Excellent organizational, documentation, and communication skills.
- Detail-oriented and quality-focused mindset.
💰 Salary & Employee Benefits
- Competitive base salary matching industry standards for mid-level CRO professionals.
- Hybrid working environment in Hyderabad offering flexibility.
- Direct exposure to international clinical trials and global study teams.
- Structured professional training and technical development programs.
- Collaborative and inclusive workplace culture.
To learn about typical roles and career progressions in clinical trial site operations, read our comprehensive Clinical Research Coordinator (CRC) Guide.
🌟 Why Join Syneos Health?
- Syneos Health is a top-tier global CRO and biopharmaceutical solutions organization supporting drug development pipelines worldwide.
- Provides a structured learning environment to build expertise in advanced document management platforms and clinical operations.
- Excellent career progression and international clinical research exposure.
📑 Resume Tips for TMF Roles
- Highlight your specific experience in eTMF databases and TMF Reference Model compliance.
- Specify any experience with document QC, completeness reviews, or site coordination.
- Keep your resume clean, structured, and optimized for ATS systems.
🎯 Syneos Health TMF Specialist Interview Questions
- What is a Trial Master File (TMF) and what is its role during clinical trial audits?
- Explain the difference between a paper TMF and an electronic TMF (eTMF).
- How do you perform a completeness review of study documents?
- What are the DIA TMF Reference Model zones?
- How do you resolve document discrepancies with clinical study teams?
📌 How to Apply?
Interested and eligible candidates can submit their applications online directly through Syneos Health's official Workday job portal using the link below. The application deadline is **July 3, 2026**. For step-by-step guidance on setting up your application profile, read our guide on how to apply for healthcare and pharma jobs online.
🚀 Apply Now
Apply Online❓ Frequently Asked Questions
Q. What is the application deadline?
The application window is scheduled to close on July 3, 2026.
Q. Who is eligible to apply?
Candidates holding B.Sc, M.Sc, B.Pharm, M.Pharm, or BDS with 1+ years of TMF or clinical research experience.
Q. What is the work model?
This is a full-time hybrid position located in Hyderabad, India.
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