Overview

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.

Pay Scale Information

USD $70,304.00 - USD $99,341.00

CHLA values the contribution each Team Member brings to our organization. Final determination of a successful candidate's starting pay will vary based on a number of factors, including, but not limited to, education and experience within the job or the industry. The pay scale listed for this position is generally for candidates who meet the specified qualifications and requirements listed on this specific job description. Additional pay may be determined for those candidates who exceed these specified qualifications and requirements. We provide a competitive compensation package that recognizes your experience, credentials, and education alongside a robust benefits program to meet your needs.