Clinical Research Nurse II, Cancer

Position:
Clinical Research Nurse II, Cancer

Location:

Boston, MA

Schedule:

40 hours per week

ABOUT BMC:

At Boston Medical Center (BMC), our diverse staff works together for one goal - to provide exceptional and equitable care to improve the health of the people of Boston. Our bold vision to transform health care is powered by our respect for our patients and our commitment to ensure everyone who comes through our doors has a positive experience.

You'll find a supportive work environment at BMC, with rich opportunities throughout your career for training, development, and growth and where you'll have the tools you need to take charge of your own practice environment.

POSITION SUMMARY:

The Clinical Research Nurse II (CRN II) will report directly to the Medical Director (MD) of the Cancer Clinical Trials Program and the Administrative Director in Hematology and Medical Oncology. The CRN II is primarily responsible for performing clinical and patient-facing tasks for patients on study. Will work with providers to identify potentially eligible patients for open clinical trials, and meet with potential research subjects to review consent forms and discuss trial requirements.

Will see patients during required study visits and, partnering with the clinical research coordinator, ensure compliance with study requirements. The Clinical Research Nurse will also provide clinical perspective and information to regulatory coordinators as needed to facilitate trial activation.

As clinically facing research staff, it is expected that the Clinical Research Nurse will spend the majority of their time in clinic seeing active study patients and will be expected to follow and evaluate 4-6 patients per day 4 days/week (16-24 patients per week).

JOB RESPONSIBILITIES

Administrative:

* Assists principal investigator with clinical trial protocol review process and protocol development as appropriate.

* Collaborates with the quality assurance of clinical trials in developing protocol specific materials.

Research:

* Assists with recruitment and registration of patients to clinical trials.

* Coordinates scheduling of patient's laboratory and radiographic assessments, admissions and clinic visits. Monitors test results as appropriate.

* Coordinates with clinical research coordinators and collaborates with staff within respective disease groups and with outside organizations in the completion of clinical research trials.

Clinical:

* Coordinates study enrollment, protocol treatment, and completion of study requirements for patients participating in clinical trials.

* Collaborates with Care Coordination for all patient care referrals. Collaborates with primary nurse (infusion, radiation, surgical) in assuring that patient care needs are met.

* Provides protocol education to patients and families; adapts interactions based on age-specific, cultural and other needs of the patient.

* Completes orders required specimens for analysis and monitors test results, as appropriate. Administers medications as necessary

* Documents in charts as appropriate and communicates observations and findings to protocol investigator and attending physicians.

* Provides protocol in-service training and serves as a resource to the health care team. Monitors the environment of care with attention to patient safety, and assures compliance with regulatory agency standards.

* Maintains clinical practice that is evidence-based and consistent with nursing policies, procedures, licensure/registration requirements, and professional scope and standards.

* Fosters an environment that is sensitive to the needs of diverse populations, including but not limited to culture, ethnicity, gender, and age.

Professional Development:

* Identifies areas for professional growth. Formulates professional goals, objectives and methods for accomplishing these.

* Pursues active membership of local and national professional organizations.

* Participates in committees as necessary.

* Meets all annual evaluation requirements and competencies within the established time period.

* Collaborates in preparing professional reports, articles, and presentations for colleagues and the public.

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