Clinical Research Coordinator-RN (In Person)
Newport Beach, CAFull-time
50 an hour
Behavioral Health Market Context
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Job Description
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.
COMPENSATION: $50/HR
Local Contract, 13 weeks ( renewable)
This is an in-person position, remote is not available
Schedule: Mon-Fri 8:30am-5pm
Required Skills & Experience:
-Two (2) or more years of any experience in cell therapy, CAR-T Trials, inpatient management experience, etc.
Required Certifications & Licensure:
-Current RN License to practice in the State of California.
-Current BLS Certification.
Apply online and send BLS card to [email protected] if you are interested
COMPENSATION: $50/HR
Local Contract, 13 weeks ( renewable)
This is an in-person position, remote is not available
Schedule: Mon-Fri 8:30am-5pm
Required Skills & Experience:
-Two (2) or more years of any experience in cell therapy, CAR-T Trials, inpatient management experience, etc.
Required Certifications & Licensure:
-Current RN License to practice in the State of California.
-Current BLS Certification.
Apply online and send BLS card to [email protected] if you are interested
Qualifications
- •Two (2) or more years of any experience in cell therapy, CAR-T Trials, inpatient management experience, etc
- •Required Certifications & Licensure:
- •Current RN License to practice in the State of California
- •Current BLS Certification
Benefits
- •COMPENSATION: $50/HR
- •Local Contract, 13 weeks ( renewable)
- •This is an in-person position, remote is not available
Responsibilities
- •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
- •Schedule: Mon-Fri 8:30am-5pm
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