- Licensure as a Registered Nurse (RN) in the State of North Carolina required.
- Must complete the CITI certification for Human Subject Research if not already completed and any additional required WakeOne training for research coordinators.
- Works under the direction/supervision of the Study Investigators, Disease Team Chair, and the Clinical Research Nurse Manager. Also receives supervision and mentoring from the Nurse Team Leader.
- Knowledge and understanding of policies, procedures, and regulations governing human subject's research and incorporates them in the conduct of research and care of participants.
- Actively screens Burn/Trauma patients for protocol enrollment, reviewing pathology, laboratory results, scans and physician notes to verify patient eligibility.
- Independently uses and documents the nursing process to plan, deliver and evaluate goal focused, individualized, safe, age-specific care as it relates to uncomplicated research participants and with assistance for complicated research participants.
- Carrying through Study protocol interventions (ultrasound, administering study medication, blood draws, responding to Level 1 Trauma Codes, Operating Room protocol, coordinating study visits and procedures, etc.).
- Coordinates patient schedules and provides information for a successful visit to meet the required protocol procedures, data collection time points and nursing care.
- With supervision, manages dose modifications and/or other modifications of the treatment regimen made in response to toxicity, pharmacokinetics, and tissue studies.
- Serves as a nursing expert of specialized patient care, including direct patient care, assessment, documentation, treatment intervention and patient/family education and support in accordance with education/experience, established policies and procedures, and state licensure requirements.
- Interaction with critically ill Trauma/Burn victims and their families.
- Follows care of protocol patients while on protocol treatment to include the following: a. Coordinates with the physician and clinic staff to assure that all protocol requirements are scheduled and ordered b. Reviews EPIC/WakeOne to ensure protocol compliance and appropriate data collection; verify that all appropriate labs and measurements are performed and ordered correctly c. Ensures that charts are clearly labeled for the appropriate drug d. Assesses and enter the initial adverse event report and serious adverse events into the eIRB system e. Follows-up with the assigned regulatory contact to resolve any outstanding reporting requirements in a prompt and appropriate manner f. Provides constant communication with the assigned protocol specialist/data manager for all event reporting and for all needed data points g. Links research encounters appropriately to facilitate the correct invoicing of research specific activities.
- Attends relevant investigational and professional meetings to keep abreast of current developments in the field.
- Serves as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and representatives of professional organizations, participant advocates, and public responsible for, or concerned about, protections for human participants of research.
- Performs other related duties incidental to the work described herein.
- 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
- Fast paced, long hours, ability to deliver results
- Professionalism and customer service skills being a must at all times
- Occasionally subject to irregular hours
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Clinical Studies RN II, Surgery Trauma - Winston Salem, United States - Atrium Health
Description
Overview
JOB SUMMARY
Provides specialized nursing care/treatment to a specific group of patients who are participating in clinical research studies within the Surgery/Trauma department of Atrium Health Wake Forest Baptist. 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. Cross trains to support the other Clinical Studies Nurses when needed.
EDUCATION/EXPERIENCE
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. Bachelor's degree in Nursing with two or more years of nursing experience preferred.
LICENSURE, CERTIFICATION, and/or REGISTRATION
ESSENTIAL FUNCTIONS
SKILLS/QUALIFICATIONS
WORK ENVIRONMENT
