Clinical Research Coordinator RN – Oncology Clinical Trials (Quick Offer)
60–75 an hour
Behavioral Health Market Context
Apply Nowvia Glassdoor
Benefits
Health InsuranceDental CoveragePaid Time Off
Job Description
Coordinator with strong regulatory knowledge and hands-on patient care experience.
You will play a key role in managing clinical studies, ensuring compliance, and delivering high-quality care to patients participating in innovative cancer research.
Key Responsibilities
• Coordinate and manage oncology clinical trials (Phase I–IV)
• Ensure compliance with ICH-GCP, FDA regulations, and IRB guidelines
• Perform patient screening, recruitment, enrollment, and informed consent
• Lead study start-up activities and protocol review
• Collect, track, and manage clinical and lab data
• Maintain regulatory documentation and study binders
• Monitor and report Adverse Events (AE/SAE)
• Complete Case Report Forms (CRFs) and resolve data queries
• Coordinate study visits, procedures, and follow-ups
• Support budgeting, cost tracking, and research operations
• Collaborate with physicians, sponsors, and cross-functional teams
• Mentor junior Clinical Research Coordinators (as needed)
Required Qualifications
✔ Active RN License – California
✔ 2+ years of clinical research experience OR equivalent
✔ Strong knowledge of:
• ICH-GCP guidelines
• FDA regulations
• Human subject protection
✔ Experience with:
• Clinical trial coordination
• Patient care in research setting
• Data management & documentation
✔ Proficiency in Microsoft Office (Word, Excel, PowerPoint)
✔ Strong communication, organization, and multitasking skills
Experience with:
• Oncology clinical trials
• IRB submissions & regulatory processes
• Electronic Data Capture (EDC) systems
• NIH / OHRP compliance
Work Environment
• Onsite clinical research setting
• Collaborative, multidisciplinary team
• Fast-paced oncology research environment
Why Apply?
✔ Competitive hourly pay ($60–$70/hr)
✔ Direct hire – stable, long-term opportunity
✔ Work on cutting-edge oncology trials
✔ Career growth in clinical research
BI01
Clinical Research Coordinator, CRC RN, Research Nurse, Clinical Trials Coordinator, Oncology RN, Clinical Research RN, GCP, FDA Regulations, IRB, Phase I-IV Trials, Patient Enrollment, Informed Consent, AE SAE Reporting, Data Management, Regulatory Compliance
Apply Now
Submit your updated resume today
Quick interview process – fast hiring decisions
Job Type: Contract
Pay: $60.00 - $75.00 per hour
Expected hours: 40 per week
Benefits:
• Dental insurance
• Paid time off
• Referral program
• Vision insurance
Work Location: In person
You will play a key role in managing clinical studies, ensuring compliance, and delivering high-quality care to patients participating in innovative cancer research.
Key Responsibilities
• Coordinate and manage oncology clinical trials (Phase I–IV)
• Ensure compliance with ICH-GCP, FDA regulations, and IRB guidelines
• Perform patient screening, recruitment, enrollment, and informed consent
• Lead study start-up activities and protocol review
• Collect, track, and manage clinical and lab data
• Maintain regulatory documentation and study binders
• Monitor and report Adverse Events (AE/SAE)
• Complete Case Report Forms (CRFs) and resolve data queries
• Coordinate study visits, procedures, and follow-ups
• Support budgeting, cost tracking, and research operations
• Collaborate with physicians, sponsors, and cross-functional teams
• Mentor junior Clinical Research Coordinators (as needed)
Required Qualifications
✔ Active RN License – California
✔ 2+ years of clinical research experience OR equivalent
✔ Strong knowledge of:
• ICH-GCP guidelines
• FDA regulations
• Human subject protection
✔ Experience with:
• Clinical trial coordination
• Patient care in research setting
• Data management & documentation
✔ Proficiency in Microsoft Office (Word, Excel, PowerPoint)
✔ Strong communication, organization, and multitasking skills
Experience with:
• Oncology clinical trials
• IRB submissions & regulatory processes
• Electronic Data Capture (EDC) systems
• NIH / OHRP compliance
Work Environment
• Onsite clinical research setting
• Collaborative, multidisciplinary team
• Fast-paced oncology research environment
Why Apply?
✔ Competitive hourly pay ($60–$70/hr)
✔ Direct hire – stable, long-term opportunity
✔ Work on cutting-edge oncology trials
✔ Career growth in clinical research
BI01
Clinical Research Coordinator, CRC RN, Research Nurse, Clinical Trials Coordinator, Oncology RN, Clinical Research RN, GCP, FDA Regulations, IRB, Phase I-IV Trials, Patient Enrollment, Informed Consent, AE SAE Reporting, Data Management, Regulatory Compliance
Apply Now
Submit your updated resume today
Quick interview process – fast hiring decisions
Job Type: Contract
Pay: $60.00 - $75.00 per hour
Expected hours: 40 per week
Benefits:
• Dental insurance
• Paid time off
• Referral program
• Vision insurance
Work Location: In person
Qualifications
- •✔ Active RN License – California
- •✔ 2+ years of clinical research experience OR equivalent
- •ICH-GCP guidelines
- •FDA regulations
- •Human subject protection
- •Clinical trial coordination
- •Data management & documentation
- •✔ Proficiency in Microsoft Office (Word, Excel, PowerPoint)
- •✔ Strong communication, organization, and multitasking skills
- •Oncology clinical trials
- •IRB submissions & regulatory processes
- •Electronic Data Capture (EDC) systems
- •NIH / OHRP compliance
Benefits
- •Pay: $60 – $70/hour
- •✔ Competitive hourly pay ($60–$70/hr)
- •✔ Direct hire – stable, long-term opportunity
- •Pay: $60.00 - $75.00 per hour
- •Expected hours: 40 per week
- •Dental insurance
- •Paid time off
- •Referral program
- •Vision insurance
Responsibilities
- •Schedule: Monday–Friday | 8:30 AM – 5:00 PM
- •This role is ideal for a Research Nurse / Clinical Trials Coordinator with strong regulatory knowledge and hands-on patient care experience
- •You will play a key role in managing clinical studies, ensuring compliance, and delivering high-quality care to patients participating in innovative cancer research
- •Coordinate and manage oncology clinical trials (Phase I–IV)
- •Ensure compliance with ICH-GCP, FDA regulations, and IRB guidelines
- •Perform patient screening, recruitment, enrollment, and informed consent
- •Lead study start-up activities and protocol review
- •Collect, track, and manage clinical and lab data
- •Maintain regulatory documentation and study binders
- •Monitor and report Adverse Events (AE/SAE)
- •Complete Case Report Forms (CRFs) and resolve data queries
- •Coordinate study visits, procedures, and follow-ups
- •Support budgeting, cost tracking, and research operations
- •Collaborate with physicians, sponsors, and cross-functional teams
- •Mentor junior Clinical Research Coordinators (as needed)
- •Patient care in research setting
- •Onsite clinical research setting
- •Collaborative, multidisciplinary team
- •Clinical Research Coordinator, CRC RN, Research Nurse, Clinical Trials Coordinator, Oncology RN, Clinical Research RN, GCP, FDA Regulations, IRB, Phase I-IV Trials, Patient Enrollment, Informed Consent, AE SAE Reporting, Data Management, Regulatory Compliance
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