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Medpace

Study Start-Up Pro: Regulatory Submissions & Site Activation

Medpace, Irving, Texas, United States, 75084

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A leading clinical research organization in Dallas, TX, seeks a full-time Regulatory Submissions Coordinator to join their Study Start-up team. The role demands excellent organizational and communication skills and involves maintaining quality in trial documents, collecting regulatory submissions, and fostering compliance. Ideal candidates will have a Bachelor's degree in a Life Sciences field and 1 to 5+ years of relevant experience. This position offers a competitive compensation package and numerous employee perks, including flexible work and health initiatives. #J-18808-Ljbffr