Clinical Research Coordinator
On-site · Los Angeles, California, United States or Beverly Hills, California, United States
Job Summary
Clinical Research Coordinator to manage assigned oncology trials, working closely with clinical research coordinators, the research director, and investigators to ensure protocol adherence and smooth study conduct. Responsibilities include coordinating subject scheduling and visits per protocol, creating and maintaining subject charts, managing EMR and CTMS data, entering data into eCRFs, preparing for monitoring visits, uploading radiology scans, maintaining trial-supply inventories, assisting with patient recruitment and enrollment, understanding clinical research billing, coordinating enrollment and protocol treatment, collaborating with infusion nurses, pharmacy and investigators to meet patient care needs, and providing protocol education to patients and families. Travel to satellite sites in the Los Angeles area is required.
Required Qualifications
- Minimum 2 years of clinical research coordinator experience
- Minimum 1 year of oncology clinical research experience with an institution-based or free-standing cancer center
- Bachelor’s degree required. Major in a related field (science, healthcare, nursing) preferred
- Certified Clinical Research Professional (CCRP) is preferred
- Strong interpersonal, organizational, and communication skills are required
- Phlebotomy is a plus
Additional Requirements
- Local candidates only
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