A global staff augmentation firm is seeking a qualified candidate to manage clinical trial documentation and ensure compliance with regulatory standards. The role involves setting up and closing Trial Master Files, supporting study documentation, and working with electronic systems for regulatory submissions. The ideal candidate will have a Bachelor's degree and 3-5 years of relevant experience, with strong organizational skills and the ability to work collaboratively in an international team.
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eTMF & Regulatory Study Documents Specialist in wilmington at Unknown Company
This position is listed as full time and onsite.