Clinical Research Regulatory Specialist

This position is listed on behalf of a partner company, which manages all applications and next steps. Our partner is looking for a Clinical Research Regulatory Specialist based in the United States.

As a Clinical Research Regulatory Specialist, you will play a vital role in ensuring the accuracy, integrity, and compliance of clinical research documentation and regulatory processes. You will support clinical study activities across the research network, overseeing regulatory submissions, essential study records, investigator credentials, and ongoing documentation requirements. Working closely with investigators, research staff, sponsors, and Contract Research Organizations (CROs), you will help ensure studies meet applicable regulatory standards and established protocols. You will also contribute to study startup activities, regulatory quality assurance, and the continuous maintenance of electronic regulatory systems. This role offers the opportunity to contribute directly to the successful execution of clinical trials while supporting the development of innovative treatments. You will join a collaborative, patient-focused environment that values integrity, accountability, professional growth, and teamwork.