Clinical Research Regulatory Specialist — HIPAA & IRB

A healthcare organization in Clinton, MD, is looking for a Clinical Research Regulatory Specialist to ensure regulatory compliance for clinical studies. Key responsibilities include maintaining communication with research personnel, preparing documentation for IRBs, and managing workflows. Ideal candidates should have 3 years of clinical trials experience and a strong understanding of HIPAA. Benefits include medical, dental, vision insurance, and a 401k matching program.

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