Sr Clinical Research Coordinator - Personalized Medicine (Full Time)
DescriptionJob Summary Works independently on more complex projects/assignments. Coordinates clinical research studies on human subjects. Responsible for subject recruitment (screening, consenting support and enrollment), follow-up, data management (entry and reporting), detailed record keeping, regulatory compliance, report writing, and correspondence with investigators, IRBs, sponsors, CRO's and regulatory authorities. Responsible for new research application (including study start-up processes and requirements) and
This job listing is no longer active.
Check the left side of the screen for similar opportunities.