Registered Nurse - Oncology Clinical Research - Full Time

Jupiter Medical Center•Essex, VT

31d•Onsite

About The Position

The Clinical Research Nurse is responsible for adhering to all federal, state, and local laws and regulations pertaining to clinical trial execution. Assists with recruitment, evaluating eligibility, and registration of patients to clinical trials. Coordinates scheduling of patient’s research procedures; laboratory and radiographic assessments, admissions, and clinic visits. Coordinates study enrollment, protocol treatment, and completion of study requirements for clinical trial subjects. Provides protocol education to patients and families; adapts interactions based on the age-specific needs of the patient. Collects and prepares required specimens for analysis and monitors test results, as appropriate. Ensures source documentation of protocol eligibility, reviews adverse events, and concomitant medications, while meeting FDA Good Clinical Practice standards. Assists principal investigator with protocol development. Assists the principal investigator as appropriate with the protocol review process. Collaborates with the Research Manager in developing protocol-specific materials. Serves as backup research coordinator for National Cancer Institute, pharmaceutical-sponsored, and National Cooperative Group protocols. Collaborates with staff within AFCI and outside organizations in the completion of clinical research trials. Works collaboratively and functions as an effective member of the healthcare team.

Requirements

Current RN licensure in the state of Florida
BLS certification through the American Heart Association for Healthcare Providers.
Minimum of 2 years recent experience as an RN
At least 2 years of clinical research experience.
Trained in FDA Good Clinical Practices for research.

Nice To Haves

BSN preferred
Oncology experience preferred.
Professional nursing certification preferred (OCN, RN-BC, etc)
Experience in oncology and/or cardiology preferred.
Clinical research certification preferred.

Responsibilities

Adhering to all federal, state, and local laws and regulations pertaining to clinical trial execution.
Assisting with recruitment, evaluating eligibility, and registration of patients to clinical trials.
Coordinating scheduling of patient’s research procedures; laboratory and radiographic assessments, admissions, and clinic visits.
Coordinating study enrollment, protocol treatment, and completion of study requirements for clinical trial subjects.
Providing protocol education to patients and families; adapting interactions based on the age-specific needs of the patient.
Collecting and preparing required specimens for analysis and monitoring test results, as appropriate.
Ensuring source documentation of protocol eligibility, reviews adverse events, and concomitant medications, while meeting FDA Good Clinical Practice standards.
Assisting principal investigator with protocol development.
Assisting the principal investigator as appropriate with the protocol review process.
Collaborating with the Research Manager in developing protocol-specific materials.
Serving as backup research coordinator for National Cancer Institute, pharmaceutical-sponsored, and National Cooperative Group protocols.
Collaborating with staff within AFCI and outside organizations in the completion of clinical research trials.
Working collaboratively and functioning as an effective member of the healthcare team.