Clinical Trial Assistant

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.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 visitsWhat you bring:🔹 1+ year of experience with oncology interventional clinical trials🔹 CCRC, CCRA or CCRP certification, 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