What are the responsibilities and job description for the CLINICAL RESEARCH RN I position at H Lee Moffitt Cancer Center & Research Institute I?
- Tampa, FL
- McKinley Campus (MKC)
- Breast Data Mgmt
- Full Time - Day Shift - Mon - Fri, 8-4:30
- Req #: 83264 Posted: February 24, 2025 -->
At Moffitt Cancer Center, we strive to be the leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer. Our diverse team of over 9,000 are dedicated to serving our patients and creating a workspace where every individual is recognized and appreciated. For this reason, Moffitt has been recognized on the 2023 Forbes list of America’s Best Large Employers and America’s Best Employers for Women, Computerworld magazine’s list of 100 Best Places to Work in Information Technology, DiversityInc Top Hospitals & Health Systems and continually named one of the Tampa Bay Time’s Top Workplace. Additionally, Moffitt is proud to have earned the prestigious Magnet® designation in recognition of its nursing excellence. Moffitt is a National Cancer Institute-designated Comprehensive Cancer Center based in Florida, and the leading cancer hospital in both Florida and the Southeast. We are a top 10 nationally ranked cancer center by Newsweek and have been nationally ranked by U.S. News & World Report since 1999.
Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join our committed team and help shape the future we envision.
Summary
The Breast Data Management program in the Clinical Trials Office is looking for a Clinical Research RN I.
Position Highlights:
- Maintains sound conduct of the clinical trial, including but not limited to recruitment, screening, education, enrollment, treatment and follow-up of eligible subjects according to protocol requirements.
- Performs nursing assessments and triages patient care needs specifically related to research protocol requirements.
- Reviews and documents appropriately patient episodes of care information specifically related to research requirements.
- Review with the principal investigator the inclusion/exclusion criteria, overall structure, and requirements for each protocol.
- Assess and document subject compliance with study treatment/protocol requirements.
- Ability to exercise independent judgment to facilitate optimal patient care.
- Organizational management of all aspects of the clinical trial, including, but not limited to, timeliness in completing case report forms, data entry, reporting adverse drug experiences, managing caseload and managing patient/data study files.
Credentials and Qualifications:
- BSN from an ACEN or CCNE accredited institution with at least one year of relevant experience or ASN from an ACEN or CCNE accredited institution with 3 years of relevant experience.
- Current Florida RN License
- One year of oncology experience and research experience preferred
- Ability to plan, organize, and coordinate multiple work assignments.
- Ability to establish and maintain effective, collaborative working relationships with others.
- Ability to clearly communicate verbally and in writing.
