Clinical Trials Activation Coordinator

To support the nation's largest cancer clinical trials program, the full-time Clinical Trials Activation Coordinator will ensure compliance for clinical research studies by coordinating the feasibility review process, preparing regulatory documents, and collaborating with sponsors and research teams, all while working remotely. Key responsibilities Serve as primary liaison for feasibility review processes for Phase I-V clinical trials Maintain regulatory documentation and ensure compliance with clinical research regulations Collaborate with research teams and sponsors to address start-up issues and facilitate site selection meetings Required qualifications Bachelor's degree required; Master's degree preferred One year of experience in regulatory compliance or quality assurance required Experience with feasibility reviews and clinical trial start-up activities preferred Preferred certifications include CCRP, CCRC, or CHRC