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Clinical Studies RN II, Surgery Trauma
Winston Salem, NC, United States
Job ID: R224968
Shift: Various
Job Type: Regular
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Department:
36205 Wake Forest University Health Sciences - Surgery: Trauma
Status:
Full time
Benefits Eligible:
Yes
Hours Per Week:
40
Schedule Details/Additional Information:
varies
Pay Range
$38.20 - $57.30
JOB SUMMARY
The Clinical Research Nurse II provides protocol driven nursing treatment to a specific group of patients who are participating in clinical research studies within the Trauma Surgery department of Atrium Health Wake Forest Baptist. They function as part of a research team that may consist of Investigators, Clinical Studies Coordinators, Data Managers, Regulatory Coordinators, and other Staff. Under the direction of the Investigator, the Clinical Research Nurse II is responsible for subject recruitment, eligibility, enrollment, informed consent, subject retention, education, and protocol adherence. Clinical responsibilities include ensuring the protocol is conducted in a high-quality manner 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
An associate's degree in Nursing from an accredited School of Nursing with one year of nursing experience preferably in a related field such as research, acute care, or a specialty area is required.
A Bachelor's degree in Nursing with two or more years of nursing experience is preferred.
LICENSURE, CERTIFICATION, and/or REGISTRATION
ESSENTIAL FUNCTIONS
Works under the direction and supervision of Dr. James Holmes IV and the Study Investigators. Also receives supervision and mentoring from the Study Team.
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 and Trauma patients for eligibility.
Actively carries out Study protocol interventions (which may include ultrasound, administering study medication, drawing blood, responding to Level 1 Trauma Codes, familiarity with 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.
Interacts with critically ill Trauma and Burn victims and their families.
Coordinates with the physician and clinic staff to assure that all protocol requirements are scheduled and ordered.
Reviews Electronic Medical Record to ensure protocol compliance and appropriate data collection.
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
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 others.
Performs other related duties incidental to the work described herein.
SKILLS/QUALIFICATIONS
WORK ENVIRONMENT
Our Commitment to You:
Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more - so you can live fully at and away from work, including:
Compensation
Benefits and more
About Advocate Health
Advocate Health is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation's largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.
Clinical Studies RN II The Clinical Research Nurse II works on multiple Trauma Studies including burn studies, Level One Trauma studies, Ventilator related Studies, and Pediatric Studies. The Studies involve going to the Operating Room, Intensive Care Units, Trauma Clinic and or the Emergency Department. None of these studies are funded by grants, they are industry, NIH and Department of Defense funded. Some of the studies are investigator initiated and others are industry sponsored. Short Description for Internal Candidates The Clinical Research Nurse II provides specialized nursing care to a specific group of patients who are participating in clinical research studies within the Trauma Surgery Department of Atrium Health Wake Forest Baptist. They function as part of a research team that may consist of Investigators, Clinical Studies Coordinators, Data Managers, Regulatory Coordinators, and other Staff.
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