Clinical Research Nurse II, Norris Cotton Cancer Center Details

Clinical Research Nurse II, Norris Cotton Cancer Center

Dartmouth-Hitchcock - Lebanon, NH

Employment Type : Full-Time

The Clinical Research Nurse (CRN) at the Norris Cotton Cancer performs a variety of clinical and non-clinical tasks associated with conducting clinical research, and within the scope of licensure. They work closely with research participants and their families to provide care, education and support throughout the trial; including clinical assessments, symptom management, and referrals. Care coordination involves a combination of in-person clinical visits and telephone triage. The CRN also collaborates with research and non-research staff, maintaining involvement throughout the clinical trial process. This is accomplished through participation in tumor boards, multidisciplinary team meetings, site initiation visits, and more.
Responsibilities:

• Provides patient care to inpatients and outpatients receiving investigational therapy.

• Screening and recruiting potential study subjects.

• Educates patient and family regarding investigational therapy in collaboration with the medical plan of care.

• Ensures that patients are scheduled for study follow-ups and for periodic testing required by the study protocol.

• Coordinates the data collection process for studies and processes forms accordingly.

• Assists in the preparation and administration of investigational agents and other medication per research protocol.

• Ensures security of study supplies and study documentation.

• Coordinates specimen collection. Records and maintains data for the research studies.

• Evaluates research patients for drug and/or disease-related toxicities and symptoms.

• Coordinates and communicates protocol-related treatment plans to other health professionals.

• Educates healthcare professional regarding investigational research protocols.

• Coordinates with the research team to address patient care delivery issues and quality improvement efforts.

• Reviews new protocols for feasibility and makes recommendations.

• Assists with the preparation and submission of study protocols, consent forms, and other study documentation to departmental research groups and the Institutional Review Board (IRB).

• Performs other duties as required or assigned.

• Graduate from an accredited Nursing Program required.
• Previous knowledge of clinical research based on study protocols preferred.
• Awareness of ethical consideration regarding investigational research studies.
• Excellent interpersonal and communication skills required.

• Licensed Registered Nurse in New Hampshire required.
• Basic Life Support (BLS) Certificate required.

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