Clinical Research Registered Nurse Cancer Center

Work Status Details: REGULAR FULL TIME | 80.00 Hours Every Two Weeks

Shift: Days
Pay Rate Type:
Annual Salary

Location:

Cancer Center

Listed is the base hiring salary range offered for this position. Actual salaries may vary depending on factors, including but not limited to skills and experience. The salary range listed is just one component of the total rewards/compensation package offered to candidates.
Min = $75,504.00
Mid = $98,155.20
Max = $

The Clinical Research Nurse, under the guidance and supervision of the Principal Investigator, coordinates study activities throughout the trial to assure that the integrity and quality of the clinical research trial is maintained and that the trial is conducted in accordance with federal, state and local regulations, sponsor protocol and other sponsor requirements, institutional policies and good clinical practice (GCP) guidelines.

The Research Nurse may assist in the design of the clinical research.

• Maintain knowledge and understanding of federal and international regulations and guidelines and institutional policies governing human subject research and incorporate them in the conduct of research and care of participants.
• Ensure that studies are conducted in full compliance with FDA Regulations and Guidelines, GCP, sponsor requirements, protocol, and institutional practices.
• Conduct training for the performance of the procedures required of each study protocol.
• Identify and procure the equipment and supplies needed to fulfill protocol requirements.
• Provide direct nursing services for study procedures as required by the study protocol.
• Evaluate patients for enrollment in clinical research studies following ethical practices and institutional policies.
• Work with the principal investigator and clinical research study team (coordinators, pharmacy, technology, etc.) to appropriately report and follow adverse and serious adverse events.
• Facilitate or oversee the data requirement for electronic case report forms by following ALCOA principles.
• Document manage study protocol and all supporting documents.
• Participate in periodic monitor visits from sponsor, regulatory authorities and other agencies.
• Perform packaging and ship study medication and specimens (blood, urine, etc.) to the sponsor or laboratory in accordance with IATA and sponsor shipping guidelines.
• Complete Subject orders in the Electronic Health Record (EHR).
• Perform procedures for clinical research studies such as collecting data (e.g., vital signs), diagnostic tests (e.g., EKG), obtaining specimens (e.g., blood, urine, etc.).
• Other duties as assigned.

Essential:

• Registered Nurse (RN)
• BASIC LIFE SUPPORT (BLS)
• ADVANCED CARDIAC LIFE SUPPORT (ACLS)

Essential:

• Bachelor's Degree

Arizona or compact state RN License; BCLS;
Advanced Life Support certification;
Bachelor’s Degree in Nursing or equivalent.

Certified discipline specific; ACRP or CCRP certified.
Phlebotomy experience preferred or completion of course within three months of position start.
Computer skills and dexterity required for data entry and retrieval of patient information.
Proficiency with Windows-style applications and keyboard.
Oncology certification or obtain within two years in role.
Five or more years of experience in oncology.
Three years of oncology experience in interventional clinical research trials.
Master’s Degree in Nursing.
Experience with EHR, EPIC preferred; CTMS system preferred.