Travel Nurse Level II RN - Research / Clinical Research - $1,881 per week

Integrated Healthcare Services is seeking a travel nurse RN Research / Clinical Research Level II for a travel nursing job in Newport Beach, California.Job Description & RequirementsSpecialty: Research / Clinical ResearchDiscipline: RNDuration: 9 weeks40 hours per weekShift: 8 hours, daysEmployment Type: TravelJob 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 Hoag 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 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.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.QUALIFICATION/LICENSUREWork Authorization : US CitizenPreferred years of experience : 2 yearsTravel required : No travel requiredShift timings : DaysIntegrated Healthcare Services Job ID #36834603. Pay package is based on 8 hour shifts and 40 hours per week (subject to confirmation) with tax-free stipend amount to be determined. Posted job title: Clinical Research Coordinator-RN II