Want to play a direct role in groundbreaking cancer research? We’re partnering with a top company to find a Research Coordinator who will run assigned oncology clinical trials from start to finish, under the guidance of the Clinical Trial Management team.
Candidates should take the time to read all the elements of this job advert carefully Please make your application promptly.
What you’ll do:
Screen, recruit and enroll patients using EMR, EDC and CTMS
Coordinate patient visits, tests and results according to each protocol
Enter data within 24 hours and resolve queries within 5 days
Report adverse events and protocol deviations within 24 hours
Manage study kits, track study drug accountability, and process and ship specimens
Work with PIs, sponsors, IRBs and the wider care team, and support audits and monitoring visits
What you bring:
1+ year of experience with oncology interventional clinical trials
CCRC, CCRA or CCRP certification, xhqgsiq or 4+ years of oncology trial experience
Working knowledge of ICH-GCP, FDA, IRB and HIPAA requirements
Strong organization and communication skills, and the ability to handle many tasks at once
A plus: regulatory experience, plus experience using a centrifuge and handling specimens
Clinical Trial Assistant in freehold at Unknown Company
This position is listed as full time and onsite.