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Advocate Health Care Logo Advocate Health Care · Nursing

Clinical Studies Registered Nurse II

United States, Winston Salem 38.20 - 57.30 USD / Hour · Job Posted February 10, 2026
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Job Description

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
  • Educational Assistance Program
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