The senior research coordinator will be expected to support an investigator initiated multi-site clinical trial. This position will independently help with the setup and startup of the study and then onboarding new sites. They will also be responsible for TCH study activities which include (but are not limited to) screening, enrollment, compensation reimbursement, scheduling visits, writing and overseeing regulatory requests (i.e. IRBs, consent forms, etc.), data entry and monitoring of research participants. Ensures accurate data collection and compliance for all sites, documentation, organization and safety of research participants.
