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Clinical Research Coordinator 1

A company is looking for a Trial Master Files Representative to manage and maintain Trial Master Files for clinical studies. Key Responsibilities Prepare and ensure the completeness of Trial Master Files (TMF) for internal and external studies Maintain the TMF, including creating file structures and indexing contents Communicate with client Sponsors and study contacts to ensure compliance with protocol and regulatory requirements Required Qualifications Bachelor's degree in a related field such as science, nursing, or other biomedical discipline Experience in clinical research and/or Trial Master Files preferred Minimum of 1 year of document management experience Proficient computer skills, including MS Word, Excel, and PowerPoint

tocol and regulatory requirements Required Qualifications Bachelor&#39;s degree in a related field such as science, nursing, or other biomedical discipline Experience in clinical research and/or Trial Master Files preferred Minimum of 1 year of document management experience Proficient computer skills, including MS Word, Excel, and PowerPoint

Trial Master Files Specialist

Trial Master Files Specialist

Behavioral Health Market Context

Job Description

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