Clinical Research Compliance Lead
Listed on 2026-10-06
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Science
Clinical Research
The Geneva Foundation seeks a Regulatory Compliance Coordinator to prepare, submit, and maintain regulatory documents for clinical research projects. You will liaison with project teams, develop recordkeeping systems, and support investigators with IRB submissions and annual reports.
You will apply knowledge of ICH/GCP, FDA and OHRP requirements, manage documents, and ensure safety and confidentiality of participants. Strong communication and organizational skills are essential.
As a Clinical Research Compliance Lead, you will play an important part at The Geneva Foundation in Bethesda, MD, United States.
We appreciate your interest in this position.
Join The Geneva Foundation and contribute to our ongoing work.
Take a moment to read everything above and see whether this role is right for you.
This posting is for the Clinical Research Compliance Lead role at The Geneva Foundation, based in Bethesda, MD, United States.
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