Syneos Health TMF Specialist Jobs
- Syneos Health Hiring TMF Specialist I – Clinical Research Jobs in Hyderabad (Hybrid)
- Company Overview
- Job Role & Responsibilities
- Core Responsibilities
- Eligibility / Qualifications
- Location & Salary
- Application Process
- Frequently Asked Questions (FAQs)
- Is this role suitable for freshers?
- What is TMF in clinical research?
- What career growth can I expect?
- Is this a high-paying clinical research job?
- Summary
Syneos Health Hiring TMF Specialist I – Clinical Research Jobs in Hyderabad (Hybrid)
Syneos Health is hiring for TMF Specialist I roles in Serilingampalli, Hyderabad (Hybrid work model). This is a full-time clinical research job designed for candidates with experience in Trial Master File (TMF) operations, clinical documentation, and regulatory compliance.
This opportunity is ideal for professionals with 1+ years of experience in clinical research, eTMF systems, or Clinical Research Coordinator (CRC) roles who want to advance their careers in a global CRO environment.
Company Overview
Syneos Health is a leading global clinical research and life sciences solutions company that supports pharmaceutical and biotechnology organizations across the entire drug development lifecycle.
The company has contributed to a majority of recent FDA-approved drugs and EMA-authorized products, making it a major player in clinical trials, regulatory strategy, and commercialization services. With a strong global workforce, Syneos Health is known for innovation, operational excellence, and patient-focused research.
Job Role & Responsibilities
As a TMF Specialist I, you will manage Trial Master File (TMF) operations, ensuring compliance with global clinical trial regulations and maintaining inspection-ready documentation.
Core Responsibilities
- Process clinical study documents as per SOPs, ICH-GCP, and regulatory guidelines
- Support TMF setup, maintenance, and close-out activities
- Perform document indexing, scanning, filing, and uploading in eTMF systems
- Ensure accuracy, security, and completeness of TMF documentation
- Conduct quality review and completeness checks of trial documents
- Identify missing or incomplete TMF records and follow up with study teams
Eligibility / Qualifications
- Educational Qualification: B.Pharm, M.Pharm, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), BDS
- Minimum Experience:
- 1+ year as eTMF Specialist OR
- 2+ years as Clinical Research Coordinator (CRC) or clinical research role
- Strong understanding of clinical trial documentation and ICH-GCP guidelines
- Familiarity with medical terminology and TMF processes
- Experience with eTMF systems is preferred
- Good communication, organizational, and time management skills
Location & Salary
- Job Location: Hyderabad (Serilingampalli), Telangana, India
- Work Mode: Hybrid
- Salary Range: ₹4.5 LPA – ₹8.5 LPA (approximate based on TMF and clinical research roles in CRO industry)
Application Process
Apply directly through the official Syneos Health careers portal:
Frequently Asked Questions (FAQs)
Is this role suitable for freshers?
No, this role requires at least 1–2 years of clinical research or TMF-related experience.
What is TMF in clinical research?
TMF (Trial Master File) contains essential documents that demonstrate compliance and proper conduct of clinical trials.
What career growth can I expect?
You can grow into Senior TMF Specialist, Clinical Operations Manager, or Regulatory Affairs roles.
Is this a high-paying clinical research job?
Yes, TMF and clinical documentation roles offer competitive salaries with steady growth in CRO companies.
Summary
| Category | Details |
|---|---|
| Company | Syneos Health |
| Vacancies | TMF Specialist I |
| Required Education | B.Pharm, M.Pharm, BSc, MSc (Life Sciences, Biotechnology, Microbiology, Biochemistry), BDS |
| Experience | 1+ year eTMF or 2+ years CRC / clinical research |
To apply for this job please visit syneoshealth.wd12.myworkdayjobs.com.
