Clinical Research Coord, II
Listed on 2026-10-09
-
Healthcare
Clinical Research, Medical Technologist & Lab Technician, Medical Science -
Research/Development
Clinical Research, Medical Technologist & Lab Technician, Medical Science, Research Scientist
Job Description - Clinical Research Coord, II (MEM
010076)
Job Description
Clinical Research Coord, II - ( MEM
010076 )
Description
Title: Clinical Research Coordinator II
Location: Fountain Valley, CA
Department: Research Administration
Status: Full-time
Shift: Day
Pay Range*: $39.12/hr-$56.75/hr
Memorial Care is a nonprofit integrated health system that includes four leading hospitals, award-winning medical groups – consisting of over 200 sites of care, and more than 2,000 physicians throughout Orange and Los Angeles Counties. We are committed to increasing access to patient-centric, affordable, and high-quality healthcare; your personal contributions are integral to Memorial Care's recognition as a market leader and innovator in value-based and other care models.
Across our family of medical centers, we support each one of our bright, talented employees in reaching the highest levels of professional development, contribution, collaboration, and accountability.
Whatever your role and whatever expertise you bring, we are dedicated to helping you achieve your full potential in an environment of respect, innovation, and teamwork.
The Clinical Research Coordinator II (CRC II) is a specialized researcher responsible for providing support for clinical research protocols. The Clinical Research Coordinator II will assist the Research Administration department with all aspects of clinical research. This individual will interact with subjects, clinic and research staff, laboratory staff, radiology staff and any other medical professionals associated with our clinical research protocols.
The CRC II works both independently and with the PI, Co-Investigator(s), department, and sponsoring agencies to support and provide guidance on the administration of the compliance, financial and other related aspects of the clinical study. With limited supervision and/or guidance the CRC II facilitates study coordination including screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
The CRC II independently manages, facilitates and monitors the daily activities of multiple moderately complex clinical trials and performs a variety of duties involved in the collection, compilation, documentation and reporting of clinical research data. After hours support and coverage may be needed to adequately meet the needs of the research subject and/or adhere to the protocol recruitments. After-hours Support Staff will be compensated for his/her time providing support during these after hours.
The CRC II may assist with the training and/or mentoring of CRC I or other CRC II staff on the basics of clinical research, Good Clinical Practice (GCP), Good Documentation Practices (GDP), Standard Operating Procedures (SOPs) and other related aspects of the clinical study. The CRC II will provide appropriate and accurate direction to junior staff, when needed.
Essential Functions and Responsibilities of the Job(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).