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Hiring TMF Specialist I
🏢 Syneos Health
📍 Hyderabad (Hybrid)
⏳ 1+ Years
📂 TMF Operations
Syneos Health is hiring TMF Specialist I for clinical research documentation & Trial Master File operations. Ideal for candidates with experience in eTMF systems, CRC roles, and clinical trial documentation.
👉 Want to understand TMF & career path? Clinical Research Coordinator (CRC) Guide
📋 Job Overview
- Role: TMF Specialist I
- Location: Hyderabad (Hybrid)
- Experience: 1+ Year (eTMF) / 2+ Years CRC
- Job Type: Full-Time
- Industry: Clinical Research
📌 Key Responsibilities
- Manage clinical trial documents as per ICH-GCP
- Support TMF setup, maintenance & close-out
- Perform scanning, indexing & uploading in eTMF
- Ensure document accuracy & compliance
- Conduct TMF quality review checks
- Resolve missing/incomplete documents
📘 Learn basics: Clinical Data Standards Guide
🎓 Qualifications & Requirements
- B.Sc / M.Sc / B.Pharm / M.Pharm / BDS
- 1+ year eTMF OR 2+ years CRC
- Knowledge of TMF & clinical documentation
- Familiar with regulatory guidelines
🎯 Crack interviews: Top Interview Questions Guide
💻 Key Skills
- Trial Master File (TMF)
- eTMF systems
- Clinical documentation
- MS Office & Adobe Acrobat
- Attention to detail
🧠 Practice now: Clinical Research Quizzes
🚀 Career Growth
- Senior TMF Specialist
- Clinical Operations Lead
- Trial Master File Manager
- Clinical Project Manager
📊 Salary insights: Pharma Salary Guide
💰 Salary (Estimated)
- ₹3.5 – ₹6.5 LPA
🌍 Why Apply
- Global clinical trials exposure
- Work on FDA-approved studies
- Structured career growth
- Collaborative work environment
🚀 Job Application Link
📌 Last Date: 25 May 2026
📌 Important Note Before You Apply:
Kindly read the full job description carefully before applying. Ensure your profile aligns with Trial Master File (TMF) management, clinical document control, ICH-GCP guidelines, and quality auditing protocols before proceeding.
Kindly read the full job description carefully before applying. Ensure your profile aligns with Trial Master File (TMF) management, clinical document control, ICH-GCP guidelines, and quality auditing protocols before proceeding.
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