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Provides specialized nursing care/treatment to a specific group of patients who are participating in clinical research studies within the Wake Forest Baptist Comprehensive Cancer Center (WFBCCC). Functions as part of a research team that may consist of Investigators, Clinical Studies Coordinators, Data Managers, Regulatory Coordinators, and other Nursing Staff. Under the direction of the Investigator, the Clinical Research Nurse II is responsible for subject recruitment, eligibility, enrollment, informed consent, retention, education, and protocol adherence. Clinical responsibilities include monitoring toxicities, assessing clinical response and providing exemplary patient care while ensuring the protocol is conducted in a high-quality manner. Conducts clinical research in compliance with Clinical Protocol and Data management (CPDM) unit, State, and Federal guidelines. In addition, communicates research-related information to patients, families, nursing, and medical staff as necessary. Provides cross coverage as needed in the Cancer Center's Clinical Protocol and Data Management (CPDM) unit. Cross trains to support the other Clinical Studies Nurses when needed. Coordinates efforts related to clinical oncology studies, including investigator-initiated or investigator-initiated industry-sponsored clinical trials. Primary areas of focus are cross-departmental trials in several areas (treatment trials, supportive care, cancer prevention and control).
Job Responsibility:
Provides specialized nursing care/treatment to a specific group of patients who are participating in clinical research studies
Functions as part of a research team
Responsible for subject recruitment, eligibility, enrollment, informed consent, retention, education, and protocol adherence
Clinical responsibilities include monitoring toxicities, assessing clinical response and providing exemplary patient care while ensuring the protocol is conducted in a high-quality manner
Conducts clinical research in compliance with Clinical Protocol and Data management (CPDM) unit, State, and Federal guidelines
Communicates research-related information to patients, families, nursing, and medical staff as necessary
Provides cross coverage as needed
Cross trains to support the other Clinical Studies Nurses when needed
Coordinates efforts related to clinical oncology studies, including investigator-initiated or investigator-initiated industry-sponsored clinical trials
Requirements:
Associate's degree in Nursing from an accredited School of Nursing with one year of nursing experience, preferably in a related field, research, acute care, or a specialty area (specifically, Oncology)
Licensure as a Registered Nurse (RN) in the State of applicable state required
Must complete the CITI certification for Human Subject Research if not already completed and any additional required WakeOne training for research coordinators
Good oral, written, listening, and interpersonal and communication skills
Ability to provide indirect patient care
EPIC/WakeOne proficiency to include appropriate documentation of research notes
Basic computer skills required
Nice to have:
Bachelor's degree in Nursing with two or more years of nursing experience preferred
Documented education and/or training in the oncology field preferred
What we offer:
Paid Time Off programs
Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
Flexible Spending Accounts for eligible health care and dependent care expenses
Family benefits such as adoption assistance and paid parental leave
Defined contribution retirement plans with employer match and other financial wellness programs