Clinical Research Coordinator RN II Oncology Research
Job
Business Integra INC
Newport Beach, CA (In Person)
$132,080 Salary, Full-Time
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Job Description
Job Title-Clinical Research Coordinator RN II - Oncology Research Location - Newport Beach, CA (BI02)
Schedule :
Monday-Friday | Day Shift (based on patient schedule)Job Type :
Full-Time | Direct Hire | Onsite Job Summary We are seeking an experienced Clinical Research Coordinator RN II to support oncology clinical trials. This role is responsible for managing Phase I-IV clinical research studies , ensuring compliance with regulatory standards, and coordinating all aspects of patient-focused research activities. Key ResponsibilitiesClinical Trial Coordination Manage multiple clinical trials including drug, device, and biologic studies Perform protocol review and study start-up activities Ensure compliance with Good Clinical Practice (GCP) and regulatory guidelines Patient Interaction & Study Management Obtain and manage informed consent Conduct patient recruitment, screening, and eligibility assessments Coordinate clinical procedures and study visits Data & Regulatory Compliance Collect, document, and enter clinical research data accurately Maintain case report forms (CRFs) and resolve data queries Monitor and report adverse events Maintain regulatory binders and study documentation Laboratory & Technical Support Collect and process lab samples in accordance with required standards Ensure data integrity and protocol adherence Collaboration & Communication Coordinate with physicians, sponsors, and research teams Participate in study meetings and site initiation visits Serve as liaison between stakeholders Operational & Financial Support Assist with study budgets, cost analysis, and fund tracking Support overall research program operations Leadership & Team Support Train and mentor junior staff as needed Promote a collaborative and positive work environment Requirements 2+ years of clinical research experience Strong knowledge of: Good Clinical Practice (GCP) FDA regulations Human subject protection Experience with: Informed consent Patient recruitment & screening Data collection and reporting Strong organizational and multitasking skills Excellent communication and interpersonal skills Education & Licensure Active Registered Nurse (RN) license - California (required) BLS Certification (required) BSN or higher preferredKeywords:
- Clinical Research Coordinator, RN Clinical Research, Oncology Research Nurse, CRC RN, Clinical TrialsRN, GCP, FDA
Regulations, Human Subject Protection, Informed Consent, Patient Recruitment, Clinical Data Management, Case Report Forms, Adverse Events, Regulatory Compliance, IRB, Clinical Research Nurse, Phase I Trials, Phase II Trials, Phase III Trials, Phase IV Trials, Oncology Trials, Research RN, Healthcare Research, Clinical Study Coordinator Pay:
$52.00 - $75.00 per hour Application Question(s): Best time to reach? Email idExperience:
RN-Clinical Research Coordinator:
2 years (Required) Good Clinical Practice (GCP): 1 year (Required) FDA regulations: 1 year (Required)License/Certification:
BLS (Preferred) RN License CA -Active (Required)Work Location:
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