CLINICAL RESEARCH RN I -- MOFFITT SOUTHSHORE

Moffitt; Florida; On-site; USD 51,000 - 78,000; Full time

Job summary

Moffitt Southshore is seeking a Clinical Research RN I to coordinate opening new protocols, evaluate patients, and enroll eligible participants in cancer trials. The CRN I delivers direct patient care, educates patients, and documents according to GCP and regulatory standards.

The role collaborates with investigators, regulatory staff, and sponsors to ensure protocol compliance and proper data capture. Onsite position with competitive pay.

Qualifications

• BSN from ACEN/CCNE accredited institution with Florida RN license and 1 year nursing experience.
• ADN/ASN with Florida RN license and 3 years nursing experience.
• NPDB self-query prior to employment; no NPDB reports unless appealed.

Responsibilities

• Coordinate opening of new protocols and patient evaluation for trials.
• Register eligible patients and coordinate protocol-related care.
• Provide direct patient care and education per protocol needs.
• Maintain regulatory files and document adverse events.
• Monitor subject accruals and protocol tracking with the team.

Skills

RN license

Clinical research

Good Clinical Practice

Patient education

Education

BSN with Florida RN license or ADN/ASN with Florida RN license

Job description

CLINICAL RESEARCH RN I -- MOFFITT SOUTHSHORE - Moffitt Cancer Center### CLINICAL RESEARCH RN I -- MOFFITT SOUTHSHOREApply: Onsite: Moffitt South Shore: Full time: Posted Today: R-5090### Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer.### As the only National Cancer Institute-designated Comprehensive Cancer Center based in Florida, Moffitt employs some of the best and brightest minds from around the world. Join a dedicated team of nearly 11,000 who are shaping the future we envision. Moffitt has been recognized as a Best and Brightest Company to Work For in the Nation and is continually named one of the Tampa Bay Times’ Top Workplaces.**Summary**The Clinical Research RN I (CRN I) facilitates clinical research activity at Moffitt Cancer Center and/or affiliated institutions by leading the coordination of opening new protocols, new patient evaluation, registering eligible patients and coordinating protocol‐related care of patients enrolled on clinical trials. The CRN I is required to have an in‐depth knowledge of protocol requirements and good clinical practices as set forth by Federal regulations. As the primary resource for the protocols, the research nurse will coordinate and provide direct patient care, perform ongoing assessments, deliver patient education, and document in accordance with standards and regulatory guidelines pertaining to specified research patients enrolled onto Moffitt run clinical trials. The CRN I will act as liaison between the investigators, primary care providers, Moffitt regulatory staff and the sponsor. Along with the investigator, the CRN I will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, this position is responsible for data and source documentation, adverse experience reporting, maintenance of regulatory files in conjunction with the regulatory specialist, maintenance of subject accruals and protocol tracking.**The Clinical Research Nurse I (CRN I)** facilitates clinical research activity at Moffitt Cancer Center and/or affiliated institutions by leading the coordination of opening new protocols, new patient evaluation, registering eligible patients and coordinating protocol-related care of patients enrolled on clinical trials. The CRN I is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by Federal regulations. As the primary resource for the protocols, the CRN I will coordinate and provide direct patient care, perform ongoing assessments, deliver patient education, and document in accordance with standards and regulatory guidelines pertaining to specified research patients enrolled onto Moffitt run clinical trials. The CRN I will act as liaison between the investigators, primary care providers, Moffitt regulatory staff and the sponsor. Along with the investigator, CRN I will screen, enroll, and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the CRN I is responsible for data and source documentation, adverse experience reporting, maintenance of regulatory files in conjunction with the regulatory specialist, maintenance of subject accruals and protocol tracking.**Minimum Experience Required**Education: BSN from an ACEN or CCNE accredited institution, with a current FL RN license and one (1) year of relevant nursing experience.\\* in lieu of BSN an ADN/ASN (associate degree in nursing) from an ACEN or CCNE accredited institution with a current Florida RN license with three (3) years relevant nursing experience.An applicant for this position, who will be or is seeking Florida licensure by endorsement, must not have any National Practitioner Data Bank (NPDB) reports, **unless the applicant has successfully appealed to have their name removed from the NPDB. An applicant is encouraged to conduct a NPDB Self-Query before proceeding with an employment application:****https://www.npdb.hrsa.gov/pract/howToGetStarted.jsp****Salary Range**$37.03 - $56.53*Salary ranges posted for this position represent the expected base pay range for the role. Actual compensation may vary based on location and a variety of job-related factors, including experience, skills, education, and internal equity among Team Members in similar positions.* *We are committed to maintaining fair and equitable pay practices and regularly review compensation to ensure alignment across our workforce.*