Travel Nurse (RN) - Ambulatory Clinic

Required Skills/Experience:

• A strong foundation of clinical research knowledge is expected.
• Computer proficiency and knowledge of various EHR operating systems.
• Ability to train others in obtaining a 12-lead EKG.
• Demonstrated competency in patient education, including cardiovascular diagnoses, disease management, and interventional procedures.
• Knowledge of lab values and pulse oximetry.
• Understanding of the principles of human subject research protection.
• Knowledge of the Human Subjects / Research Subject Bill of Rights.

Preferred Skills/Experience:

• 2+ years of clinical research experience preferred.
• 3+ years of subspecialty nursing experience in an acute care/ambulatory setting preferred.
• Rheumatology, oncology, inpatient studies, and CAR-T experience are highly preferred.
• Bilingual English/Spanish communication skills are preferred.

Required Credentials:

• Cannot have any hits or suspensions on a license or any background hits from any point in the past.

Special Requests:

• RTO must be listed at time of submission.
• All positions at Providence Health & Services require that any and all lab items requested during onboarding be completed within 72 hours of signing a contract—no exceptions. Candidates must be responsive and willing to go to a lab to complete health orders as soon as possible after signing. Failure to comply may lead to a pushed start or cancellation as assessed by the facility.
• References must cover at least 1 full year of relevant experience in the specialty within the past 3 years.
• You must be able to complete labs within 48 hours of signing.

Unit Details:

• This is a patient-facing and administrative role supporting Phase 1 clinical trials centered on rheumatology patients.
• The Clinical Research RN coordinates research activities; recruits and enrolls patients; provides patient and family education about study requirements and investigational-agent risks, benefits, and side effects; obtains written informed consents; performs protocol-directed data collection; and performs regulatory functions.
• The role includes training and assisting CRC I/II as necessary, maintaining study binders and organized research records, and managing monitor visits and audits.
• Research activities are conducted in compliance with federal regulations, good clinical practice (GCP), and Institutional Review Board (IRB) guidelines.
• Study medication and supply inventory and temperature logs are maintained, and temperature excursions are promptly reported.
• CAR T-cell clinical research focuses on genetically modifying a patient's T cells to target and destroy cancer cells or treat autoimmune conditions.
• Uses IDX and PACS.

Shift & Scheduling:

• No weekends; Monday-Friday on site.

Pre-employment modules may be required for this role. Please upload any certifications or health documents you have to your profile to expedite your on-boarding process.

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