Clinical Regulatory Coordinator — IRB & Docs Expert
CenExel
CenExel Clinical Research in Gaithersburg, MD seeks a Regulatory Affairs professional to organize and implement regulatory documents for FDA-guided trials. You will coordinate submissions, trainings, and communications with sponsors, IRBs, and investigators. Ideal candidate has 0-2 years in regulatory affairs, strong R&D documentation skills, and proficiency in Excel and Word. This on-site role supports site activities with competitive benefits and a collaborative team environment. #J-18808-Ljbffr CenExel
Vacancy posted 4 days ago
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