Registered Nurse (RN) - Clinical Research Coordinator II

Integrated Resources, Inc

Newport Beach, CA

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JOB DETAILS

JOB TYPE

Contractor

SKILLS

Aviation Industry, Basic Life Support (BLS), Budget Management, Case Report Form (CRF), Clinical Assessment, Clinical Data, Clinical Practices/Protocols, Clinical Research, Clinical Trial, Clinical Trial Management, Communication Skills, Cost Analysis, Data Entry, Data Quality, Detail Oriented, Establish Priorities, FDA (Food and Drug Administration), FDA Requirements, GCP (Good Clinical Practices), Government Funding, High School Diploma, ICH Regulations, Informed Consent, Interpersonal Skills, Maintain Compliance, Mentoring, National Institutes of Health (NIH), Nursing, Nursing Credentials, Operational Support, Organizational Skills, Presentation/Verbal Skills, Project/Program Management, Record Keeping, Registered Nurse (RN), Regulatory Requirements, Site Initiation, Society of Clinical Research Associates (SoCRA), Specimens/Samples, Team Player, Time Management, Willing to Travel, Writing Skills

LOCATION

Newport Beach, CA

POSTED

29 days ago

Job Title: Registered Nurse (RN) - Clinical Research Coordinator II Job Location: Newport Beach, CA Job Duration: 2-3 Months (possibility of extension) Job Summary: The Clinical Research Coordinator-Registered Nurse II (CRC RN-II) is responsible for all aspects of clinical research activities and works in close cooperation with study physicians, inter- and intradepartmental stakeholders, and sponsors. The position is responsible for managing complex clinical research trials including drug, device, and biologic studies across Phase I, II, III, and IV clinical trials, government-funded research, and investigator-initiated studies while ensuring compliance with Good Clinical Practice standards, human subject protection regulations, and FDA guidelines. Job Responsibilities: Manages complex clinical research trials including industry-sponsored, government-funded, and investigator-initiated studies. Maintains compliance with Good Clinical Practices, FDA regulations, and human subject protection standards. Provides overall study management, coordination, and operational support for assigned research trials. Performs protocol review and preparation activities prior to study initiation. Administers and manages the informed consent process in accordance with regulatory requirements. Conducts subject recruitment, screening, and eligibility assessments based on inclusion and exclusion criteria. Collects, processes, and documents laboratory samples in compliance with International Air Transport Association standards. Ensures completion of all protocol-required clinical assessments and procedures. Accurately collects, records, and enters study data into clinical research databases while maintaining data integrity and quality. Completes case report forms and addresses data queries in a timely manner. Monitors and reports adverse events according to protocol and regulatory requirements. Maintains regulatory binders and study documentation in accordance with sponsor and regulatory standards. Develops study flow sheets and prepares study source documentation. Hosts and participates in study team meetings and site initiation visits. Assists with cost analysis, study budget preparation, and tracking and distribution of study funds. Supports the growth and strategic vision of the Client Institute for Research and Education. Assists with training and mentoring other Clinical Research Coordinators as needed. Promotes team building and fosters a positive and respectful work environment. Performs other duties as assigned. Required Education: High School Diploma. Preferred Education: Bachelor of Science in Nursing (BSN) Degree or higher. Required Certifications & Licensure: Current licensure in good standing as a Registered Nurse in the State of California. Basic Life Support (BLS) Certification. Preferred Certifications & Licensure: Current ACRP Certification. OR SoCRA Certification. Nursing Specialty Certification. International Air Transport Association (IATA) Certification. Required Skills & Experience: Two (2) or more years of experience performing clinical research duties or equivalent experience and training. Knowledge of Good Clinical Practices, protection of human subjects, and FDA regulatory guidelines. Excellent verbal and written communication skills. Strong organizational skills with close attention to detail. Excellent interpersonal skills to work effectively within a diverse team environment. Strong analytical and problem-solving skills. Proficiency in Microsoft Word, PowerPoint, and Windows-based applications. Ability to work effectively in a fast-paced, team-based environment. Project management and coordination skills with the ability to prioritize tasks and meet multiple deadlines. Ability to establish and maintain cooperative working relationships with patients, physicians, and coworkers. Ability to behave professionally in all work settings and promote team-building behaviors. Ability to follow organizational and departmental policies and procedures. Ability to travel locally between organization locations as required. Preferred Skills & Experience: Working knowledge of FDA, NIH, and OHRP regulatory requirements. Working knowledge of ICH Good Clinical Practice guidelines. Understanding of clinical trial methodologies. Experience filing Institutional Review Board documentation. Ability to abstract data from medical records and transfer information into data collection forms or electronic databases.

About the Company

Integrated Resources, Inc

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