Clinical Research Consortia Coordinator

Children's Hospital Los Angeles (CHLA); Los Angeles (CA); Hybride; USD 70 000 - 95 000; Plein temps

Résumé du poste

Children’s Hospital Los Angeles (CHLA) is seeking a Clinical Research Consortia Coordinator to independently coordinate and manage all consortia activities at the coordinating center, focusing on protocols and clinical trials in Oncology. The role requires strong site communication and compliance with study protocols.

The position is full-time, exempt, hybrid with 1-2 days on site per week, and involves collaboration with the Consortia Administrator and Medical Director to support multi-site

Qualifications

• 3+ years of hospital-based Phase 1-3 clinical trials experience focusing on consortia activities in Oncology.
• 2+ years of clinical trial data management experience.

Responsabilités

• Coordinate and manage all consortia activities at the coordinating center.
• Serve as the main contact for participating sites for protocol-related clarifications and compliance.
• Collaborate with the Consortia Administrator and Medical Director.

Connaissances

Consortia coordination

Clinical trial data management

Site communication

Formation

Bachelor’s Degree

Clinical Research Certification

Description du poste

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.