A Clinical Research Coordinator I (CRC) performs tasks to facilitate cancer clinical research.
Subject care requirements may include:
The CRC may also perform phlebotomy, specimen processing and participate in process improvement events as necessary.
Requires good medical knowledge including medical terminology, and basic subject care. May require phlebotomy skills and the ability to operate centrifuges and EKG machines. Prefer higher education or vocational training specializing in healthcare.
Minimum one year of full-time related experience. May require Healthcare Assistant Certificate or other specialized training. Previous experience in cancer clinical research is a plus.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, disability or protected veteran status.