Clinical Trials Regulatory Specialist: IRB, TMF & Compliance

Green Life Science

Green Life Science is seeking a Regulatory Affairs Specialist in Miami to manage regulatory submissions and maintain inspection-ready study files. This role requires strong regulatory experience and knowledge of FDA and ICH-GCP guidelines. The ideal candidate will have excellent organization and communication skills, with at least 2 years in a clinical research environment. Bilingual proficiency in English/Spanish is a plus. #J-18808-Ljbffr Green Life Science

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Vacancy posted 4 days ago

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