Clinical Research Consortia Coordinator

Schedule: Full-Time, Exempt. Standard Monday-Friday business hours. Hybrid with 1-2 days per week. 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. Preferred Qualifications Clinical research coordination experience.Oncology research experience preferred.Strong attention to detail with the ability to maintain accuracy in a fast-paced environment.Proven ability to manage multiple projects, priorities, and deadlines simultaneously.Excellent organizational and time management skills. 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. This is a grant‑funded position, in whole or part. Terms and conditions of employment are contingent upon the availability of grant funding, which may be subject to change without notice.