Clinical Research Regulatory Specialist - Bilingual
Rovia
Rovia Clinical Research in New York seeks a Regulatory Specialist to support day-to-day regulatory activities across the site network, ensuring compliance with ICH/GCP, sponsor requirements, and Rovia SOPs. The role involves startup activities (IRB submissions, regulatory docs), managing the Florence eRegulatory platform, and collaborating with investigators to keep submissions and study files up to date. Travel about 10% to Palmetto Bay as needed. #J-18808-Ljbffr Rovia
Vacancy posted 1 day ago
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