Clinical Research Coordinator-RN II

Details Client NameHoag Hospital Newport Beach Job TypePermanent OfferingNursing ProfessionRN SpecialtyCare Coordinator Job ID35425424 Job TitleClinical Research Coordinator-RN II Shift Details ShiftDay - 8x5 - 09AM Scheduled Hours40 Job Order Details Start Date04/20/2026 Duration0 Job DescriptionJob Title: Clinical Research Coordinator - Registered Nurse II Profession: Clinical Research Coordinator Specialty: RN II Duration: Direct Hire Shift: Onsite Only Hours per Shift: 40.00 Experience: Two (2) or more years of experience performing clinical research duties or equivalent experience and training. License: Current licensure in good standing as a Registered Nurse in the State of California. Certifications: Basic Life Support (BLS) Certification. Must-Have: - Excellent analytical and problem-solving skills. - Excellent verbal and written communication and presentation skills. - Excellent organizational skills with close attention to detail. - Excellent interpersonal skills to work effectively in a diverse team. - Ability to work effectively in a fast-paced, team-based environment. - Project management and coordination skills. - Ability to prioritize tasks and meet multiple deadlines on concurrent projects. - Ability to establish cooperative working relationships with patients, coworkers, and physicians. - Professional demeanor in all settings and promotes team building. - Knowledge of FDA, NIH and OHRP regulatory requirements. - Understanding of clinical trial methodologies and experience filing Institutional Review Board documents. - Ability to abstract data from medical records and transfer it to data collection forms or electronic databases. - Proficiency with Microsoft Word, PowerPoint, and Windows. Description: The Clinical Research Coordinator - Registered Nurse II (CRC RN-II) is responsible for all aspects of clinical research activities. They work in close cooperation with study physicians and inter- and intradepartmental stakeholders. The position manages complex clinical research trials including drug, device, and biologic studies. They ensure compliance with Good Clinical Practice standards, human subject protection regulations, and FDA guidelines. Key responsibilities include: Managing complex clinical research trials including industry-sponsored, government-funded, and investigator-initiated studies. Maintaining compliance with Good Clinical Practices and human subject protection standards. Providing overall study management, coordination, and operational support for assigned research trials. Performing protocol review and preparation activities prior to study initiation. Administering and managing the informed consent process in accordance with regulatory requirements. Conducting subject recruitment, screening, and eligibility assessments based on inclusion and exclusion criteria. Collecting, processing, and documenting laboratory samples in compliance with established standards. Ensuring completion of all protocol-required clinical assessments and procedures. Accurately collecting, recording, and entering study data into clinical research databases while maintaining data integrity and quality. Completing case report forms and addressing data queries promptly. Monitoring and reporting adverse events according to protocol and regulatory requirements. Maintaining regulatory binders and study documentation in accordance with sponsor and regulatory standards. Developing study flow sheets and preparing study source documentation. Hosting and participating in study team meetings and site initiation visits. Assisting with cost analysis, study budget preparation, and tracking and distribution of study funds. Supporting the growth and strategic vision of the research institution. Assisting with training and mentoring other Clinical Research Coordinators as needed. Promoting team building and fostering a positive and respectful work environment. Performing other duties as assigned. Client Details Address1 Hoag Dr CityNewport Beach StateCA Zip Code92663 Job Board DisclaimerBy applying for jobs on this website, you consent to receive daily messages from CYNET about assignments that match your profile. Email or text HELP for more info, or STOP to unsubscribe.Your mobile info will not be shared with third parties for marketing. Standard messaging and data rates may apply.

Created: 2026-04-15