Clinical Research Coordinator

Highlights6 month contract with eligibility for direct hire! M - F schedule, no weekends or late nights!Work on a wide variety of studies from GI to metabolic to CNS! The CompanyOur client is a fast growing clinical research site network that started in 2015 and grew to 11 sites with plans to double in the next couple years! They have run many clinical studies in Phase I - IV in therapeutic areas mainly focused in GI, Hepatology, and CNS! Their goal is to be the best place to work in the country, and they are excited to find people excited to make that vision come to life through quality patient care and research.ResponsibilitiesAs a Contract CRC you will be a specialized research professional under the direction of the clinical Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily clinical trial activities and play a critical role in the conduct of the study including supporting patients throughout the clinical trial process!Conduct procedures such as vital signs, blood draws, EKGs, and scans.Patient recruitment, enrollment, scheduling, and consentLab procedures and shipmentsMaintain GCP and follow protocolsData management in EDC systemsOverall coordination of the studyQualifications:2+ years of experience working as a CRC on sponsor backed clinical trialsPhlebotomy experience (ability to perform without supervision)Ability to work on site M-F on site (there is no remote or hybrid days)

Created: 2025-03-03