Clinical Translational Research Coordinator
Current
Nashville, Tennessee, United States
- Manage and coordinate daily operations of multiple studies, including participant recruitment from clinical appointments and medical record chart review, scheduling, visit completeness, and compliance, ensuring.
- Maintain accurate and up-to-date documentation of trial activities, including informed consent forms, reimbursement forms, IRB, and regulatory submissions.
- Collaborate with multidisciplinary teams, including principal investigators, sponsors, and regulatory agencies, to facilitate smooth trial execution and resolve any issue that arose
- Ensure all study activities adhere to ethical guidelines and Good Clinical Practice (GCP) standards, prompting the welfare and rights of study participants.