Registered Nurse/Clinical Research Nurse (CRN)

Registered Nurse/Clinical Research Nurse (CRN)

Location: Fullerton, CA

Onsite Flexibility: Onsite

Contract Details

• Position Type: Contract
• Contract Duration: 6 months
• Pay Rate: $63.00 $67.20 / Hour (USD)
• Shift / Schedule: Day shift, 5x8 Hours, 8:00 17:00
• Work Authorization: Applicants must be authorized to work for ANY employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.

Job Summary

This is a Phase 1 Clinical Research RN role centered around Rheumatology clinical trials. This position is being posted based off a 6-month grant, and the RN will be expected to join the trial with a strong foundation of Clinical Research Knowledge. This is a great opportunity to work with a large West Coast Health System and participate in meaningful work supporting Rheumatology patients. The role is both Patient Facing & Administratively-Based.

The Clinical Research Nurse has working knowledge of clinical research activities and is responsible for the coordination of clinical research protocols, working under compliance with federal regulations, good clinical practice (GCP), Institutional Review Board (IRB) guidelines, department standard work, and performance within their scope of practice.

Key Responsibilities

Essential Functions:

• Coordinates research activities in consultation with the Investigator, Research Program Manager, protocol and sponsor in a safe, efficient and cost effective manner.
• Trains and assists CRC I/II as necessary.
• Ensures study binders for each participant in a study is complete and accurate.
• Attends investigators' meetings as required.
• Per Investigator's orders, provides patient and family education regarding study requirements, risks/benefits/side effects of investigating agents, provided information on the Investigational Subjects Bill of Rights, Use and Disclosure of Protected Health Information and obtains written informed consents.
• Performs data collection procedures as directed by the research protocol with accurate, thorough source documentation and submits data to sponsor in a timely manner.
• Networks and researches potential new studies.
• Performs regulatory functions for existing and upcoming studies.
• Works with PI and Research Program Manager for input to ultimately submit to local or central IRB.
• Recruits and enrolls patients into various studies, working with other Physicians & Allied Health Professionals across multiple departments.
• Manages monitor visits and audits.
• Consistently maintains organized record of all research activities, as required by the sponsor and standard work, including but not limited to regulatory documents, source documents, various tracking logs, and correspondence.

Additional Responsibilities:

• Ensures secure, accurate inventory of study medications/supplies.
• Ensures current temperature logs for all research medications, or delegates as appropriate and promptly reports temperature excursions to appropriate personnel.
• Participates in work groups, meetings and activities as assigned.
• Responsible for knowing their legal scope of practice and maintain clinical competence with regards to skills under license or certificate.
• Supports team effort, exhibits willingness to accomplish tasks, follows through on tasks until they are completed.
• Performs all other duties as assigned.

Age-Related Competencies:

• Demonstrates the knowledge and skills necessary to provide care appropriate to the age of the patients served including knowledge of the principles of growth and development and psychosocial characteristics and interventions for age specific requirement of the assigned unit.
• Demonstrates the ability to assess and interpret age appropriate data about the patient's status in order to identify age-specific needs and provide the care needed.
• Demonstrates age appropriate communication skills for the patient population served.
• Demonstrates knowledge of age-specific community resources.

Information Management:

• Treats all information and data within the scope of the position with complete confidentiality and security.

Risk Management:

• Cooperates fully in all risk management activities and investigations.

Required Skills

• IDX, Meditech, NextGen, PACS experience a plus
• Bilingual English/Spanish a plus

Preferred Skills

• Rheumatology experience highly preferred
• Oncology experience highly preferred
• Inpatient Studies experience highly preferred
• CAR-T experience highly preferred
• CCRC (Certified Clinical Research Coordinator) preferred

Education Requirements

• Active RN license required
• CCRC preferred

Required Experience

• Minimum 2 years of Clinical Research experience required
• Minimum 2 years of Sub Specialty Nursing Experience in an acute care/ambulatory setting required

Nice-to-Have Experience

• 3 years of Sub Specialty Nursing Experience in an acute care/ambulatory setting preferred
• 2 years of Clinical Research experience preferred (3 years preferred)

Benefits

• Medical, Vision, and Dental Insurance Plans
• 401k Retirement Fund

About the Client

This client is a leading healthcare and medical services organization operating across the West Coast, delivering high-acuity clinical and research-based care through a large regional health system. The organization employs registered nurses, clinical research coordinators, allied health professionals, and a range of specialized clinicians who collaborate across multiple departments and therapeutic areas to advance patient care and support innovative clinical trial programs.

About GTT

GTT is a minority-owned staffing firm and a subsidiary of Chenega Corporation, a Native American-owned company in Alaska. We highly value diverse and inclusive workplaces and support Fortune 500 organizations across banking, financial services, technology, life sciences, biotech, utilities, and retail sectors throughout the U.S. and Canada.

Job Number: 26-16516

Industry: Healthcare