Registered Nurse (RN) - Cancer Treatment Center
Providence Saint John’s Cancer Institute · Santa Monica, CA
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PART-TIME
Posted Nov 5, 2026
Job Description
Clinical Research Coordinator
Schedule
Full-time, 5x8 days, Days (08:00 - 17:00), Hybrid option available.
Assignment Details
Temporary to permanent position, candidate should ideally have a local commute of 30 minutes or less.
Requirements
• Minimum of five years of experience in a clinical research setting managing patients.
• Experience in patient-facing clinical trials is required.
• Blood Draw Certification is required (must be a phlebotomist, MA, LVN, or RN).
• Must possess Epic experience and strong computer skills (including Outlook, MS Teams, Word, and Excel).
• Certification as CCRC (ACRP) preferred.
• Neurological conditions experience is a plus.
• Spanish or Korean speaking skills are a plus.
Responsibilities
• Support investigators during the conduct of multiple clinical research trials.
• Coordinate enrollment, study visits, and follow-up care of patients participating in clinical trials.
• Act as the liaison between sponsors, regulatory agencies, patients, investigators, nurses, and staff during trials.
• Assist in training new research assistants and Clinical Research Coordinators as needed.
• Conduct all transactions in compliance with applicable regulations, policies, and procedures.
• Maintain professional appearance and conduct at all times.
• Maintain organizational and patient confidentiality at all times.
Benefits
• Medical, Dental, Vision Insurance After 90 Days
• Accrued PTO
• Continuing Education through TLC Academy & Relias Training
• Referral Bonus up to $1,000
• 401(k) with Match
• Access to Purchase Aflac
• Employee Assistance Program (EAP)
• Discounts on Travel and Retail through Employee Discount Network
• Life Insurance
• TLC ShiftShield income protection for eligible travelers between assignments
Compliance / Notes
Parking details will be provided.
Schedule
Full-time, 5x8 days, Days (08:00 - 17:00), Hybrid option available.
Assignment Details
Temporary to permanent position, candidate should ideally have a local commute of 30 minutes or less.
Requirements
• Minimum of five years of experience in a clinical research setting managing patients.
• Experience in patient-facing clinical trials is required.
• Blood Draw Certification is required (must be a phlebotomist, MA, LVN, or RN).
• Must possess Epic experience and strong computer skills (including Outlook, MS Teams, Word, and Excel).
• Certification as CCRC (ACRP) preferred.
• Neurological conditions experience is a plus.
• Spanish or Korean speaking skills are a plus.
Responsibilities
• Support investigators during the conduct of multiple clinical research trials.
• Coordinate enrollment, study visits, and follow-up care of patients participating in clinical trials.
• Act as the liaison between sponsors, regulatory agencies, patients, investigators, nurses, and staff during trials.
• Assist in training new research assistants and Clinical Research Coordinators as needed.
• Conduct all transactions in compliance with applicable regulations, policies, and procedures.
• Maintain professional appearance and conduct at all times.
• Maintain organizational and patient confidentiality at all times.
Benefits
• Medical, Dental, Vision Insurance After 90 Days
• Accrued PTO
• Continuing Education through TLC Academy & Relias Training
• Referral Bonus up to $1,000
• 401(k) with Match
• Access to Purchase Aflac
• Employee Assistance Program (EAP)
• Discounts on Travel and Retail through Employee Discount Network
• Life Insurance
• TLC ShiftShield income protection for eligible travelers between assignments
Compliance / Notes
Parking details will be provided.
Benefits
- Paid time off
- Dental insurance
- Health insurance
Additional Details
- City
- Santa Monica
- State
- California
- Country
- US
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