Coordinator, Clinical Research Consortia

Purpose Statement/Position Summary: The Clinical Research Consortia Coordinator independently coordinate and manage all consortia activities at the coordinating center as it pertains to consortia protocols and clinical trials in conjunction with the Consortia Administrator and Medical Director. The Consortia Coordinator will be the main contact for all other participating sites to assist with all protocol-related issues such as clarifications and compliance.



Minimum Qualifications/Work Experience: Required: 3+ years of hospital-based Phase 1-3 clinical trials experience with a focus on Consortia related activities in Oncology. 2+ years of clinical trial data management experience



Education/Licensure/Certification: Required: Bachelor’s Degree or equivalent combination of relevant education and experience may be considered, or Clinical Research Certification may be considered as a substitute for degree requirements.