In this role, you will have the opportunity to: Lead the day-to-day operations of the Internal Blood Draw Program, coordinating participant scheduling, supporting study enrollment and informed consent activities, and ensuring compliance with IRB-approved protocols, Good Clinical Practice (GCP), and HIPAA requirements. This role serves as the primary point of contact for study execution, including participant recruitment, scheduling, study enrollment, and informed consent, while ensuring compliance with Good Clinical Practice (GCP), protocol requirements, participant safety, and data integrity.