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    Hybrid TMF Specialist Job at Syneos Health, Hyderabad | Pharmacy Candidates Apply Now!

    Hybrid TMF Specialist Job at Syneos Health, Hyderabad

    Looking for a TMF Specialist I job in Hyderabad with a leading CRO? This is a great opportunity for life sciences graduates to build a career in clinical research operations. The role focuses on managing Trial Master File (TMF) documentation across the clinical trial lifecycle. Candidates will gain exposure to global regulatory standards and inspection-ready processes. This Hybrid TMF Specialist Job at Syneos Health Careers in Hyderabad is ideal for professionals with experience in clinical research or eTMF systems. Check the full details below to explore responsibilities, qualifications, and benefits.

    About the Company:

    Syneos Health is a leading, fully integrated life sciences services organization. The company partners with innovators across drug development and commercialization to accelerate progress in healthcare. With a strong global presence, Syneos Health has contributed to the development of a significant percentage of FDA-approved drugs and EMA-authorized products. It is known for its collaborative culture, innovation-driven approach, and commitment to improving patient outcomes.

    Job Details:

    • Job Title: TMF Specialist I
    • Location: Hyderabad, India (Hybrid)
    • Job Type: Full-Time (Office-based/Hybrid)
    • Job ID: 25107822
    • Application Deadline: May 25, 2026
    • Experience Required: 1+ year (eTMF) or 2+ years (CRC/clinical research)

    Key Responsibilities:

    • Support set-up, maintenance, and close-out of Trial Master File (TMF)
    • Process study documentation as per SOPs, ICH-GCP, and regulatory guidelines
    • Perform document scanning, indexing, filing, and uploading in eTMF systems
    • Ensure accuracy, security, and compliance of TMF documents at Syneos Health Careers
    • Conduct quality and completeness reviews of TMF documentation
    • Identify missing or incomplete documents using expected document lists
    • Maintain inspection-ready TMF across the clinical trial lifecycle

    Educational Requirements for this Job:

    • B.Pharm, M.Pharm

    Skills Required:

    • Knowledge of Trial Master File processes and clinical documentation
    • Familiarity with medical terminology
    • Experience with electronic TMF systems (preferred)
    • Strong communication and organizational skills
    • Attention to detail and a quality-focused mindset
    • Ability to manage multiple tasks and deadlines
    • Proficiency in Microsoft Office and Adobe Acrobat
    • Teamwork and independent working ability

    Benefits of the Hybrid TMF Specialist Job:

    • Opportunity to work with a global CRO leader
    • Exposure to international clinical trial processes
    • Career growth and development programs
    • Inclusive and collaborative work culture
    • Competitive compensation and rewards
    • Hands-on experience with global regulatory standards

    CLICK HERE TO APPLY NOW

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