Clinical Research Coordinator II - Oncology

Work Location Orange, California Work Shift Day – 08 hrs (United States of America) Job Summary The Clinical Research Coordinator II (CRC‑II) works with minimal supervision to provide coordinator support to multiple human subjects’ clinical research projects. Responsibilities include assessing feasibility of protocols, preparing regulatory review materials for IRB submission, identifying potential study participants, coordinating and collecting research data/specimens, completing study records accurately and timely, participating in quality assurance audits, managing study materials and supplies, communicating across multiple teams, and archiving records per policy. Pay Range Minimum: $30.94 • Midpoint: $40.99 • Maximum: $51.05 Qualifications Experience Required – Minimum three years of clinical research coordination experience. Preferred Experience – Oncology clinical research experience in a hospital setting and/or pediatric clinical research experience. Education Required – Associate degree or equivalent experience in lieu of education. Preferred Education – Bachelor’s degree in a relevant field. Specialized Skills Basic knowledge of Microsoft Office (Word, Excel, PowerPoint) Strong interpersonal, oral and written communication skills Detail oriented and capable of working under pressure in a fast‑paced environment while managing multiple priorities Working knowledge of human subjects’ regulatory requirements and ICH‑GCP guidelines Preferred: Ability to conduct informed consent Working knowledge of Cerner or equivalent electronic medical record system Knowledge of sample identification, processing, and storage Licensure & Certifications Required – RQI Responder (American Heart Association). If not certified at hire, certification must be obtained within six months of assuming the position. Preferred – Phlebotomy certification; Association of Clinical Research Professionals Certified Professional (ACRP‑CP); Certified Clinical Research Professional (CCRP); or Certified Clinical Research Coordinator (CCRC). Work Environment – Functional Demand Light–moderate energy level. Lift and carry 25–35 lbs. Push/pull 50–100 lbs (e.g., empty bed, stretcher). Physical Activity Requirements Bending, carrying objects, climbing, keyboard use/repetitive motion, pinching/fine motor activities, push/pull, reaching forward, reaching overhead, sitting, squat/kneel/crawl (squat & knee), standing, talking or hearing, tasting or smelling, twisting, walking, wrist position deviation Lifting (floor to waist level): constant ≥67%, frequent 36‑66%, occasional 0‑35% Lifting (waist level and above): constant ≥67%, frequent 36‑66%, occasional 0‑35% Sensory Requirements Color discrimination, depth perception, far vision, hearing, near vision. Environment Requirements Airborne communicable disease, bloodborne pathogens, chemical, dust particulate matter, extreme noise levels, extreme temperatures, radiation, uneven surfaces or elevations. Non‑Discrimination Statement CHOC does not discriminate on the basis of age, race, color, religion, national origin, ancestry, marital status, genetic information, disability, sex, gender (including pregnancy, breastfeeding, childbirth, lactation or related medical conditions), gender identity or expression, medical condition, sexual orientation, veteran status, military or uniformed service member status, or other protected characteristics in accordance with state and federal laws. CHOC will consider qualified applicants with criminal histories in accordance with the Fair Chance Initiative for Hiring. #J-18808-Ljbffr Children’s Hospital of Orange County