Regulatory Coordinator — Clinical Trials & Compliance
CenExel
CenExel Clinical Research in Gaithersburg, MD is seeking a Regulatory Affairs Coordinator to organize and implement regulatory documents for FDA-guided trials, ICH GCP adherence, and SOP-compliant processes. Manage start-up documents, IRB submissions, and trainer staff on SOPs. You will maintain regulatory documents, coordinate with sponsors, and ensure study teams stay compliant. This role emphasizes attention to detail, multi-tasking across trials, and strong communication. #J-18808-Ljbffr CenExel
Vacancy posted 4 days ago
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