Clinical Research Nurse
About The Position
This full-time Clinical Research Nurse position is within the 85190 Greater Charlotte Research and Other Sponsored Programs - Academic Internal Medicine Department, working 40 hours per week, Monday-Friday from 8 AM to 4 PM with some limited weekend call. 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. 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. The organization is focused on transformation, guided by the patient's experience, exploring new technologies for care delivery, fostering a dynamically inclusive workforce, and redefining care standards with world-class doctors, innovative solutions, outstanding outcomes, and leading-edge research and clinical trials.
Requirements
- applicable state RN licensure required
- BLS required per policy guidelines
Nice To Haves
- BSN preferred
- Clinical research experience preferred
- Certification in clinical research (SoCRA, ACRP) preferred
- IV and Phlebotomy experience preferred
Responsibilities
- Recruits, interviews and obtains informed consent from prospective subjects for entrance into clinical trials and studies.
- Coordinators appropriate laboratory tests and other procedures for subjects participating in studies; including drawing blood or collection of other samples.
- Coordinates with Investigational Pharmacy for subjects to receive required drugs.
- Communicates with Sponsored Programs Administration to ensure proper management of charges and billing.
- Coordinates and submits IRB protocols, reports, revisions, updates, approvals.
- Records appropriate clinical and laboratory data on forms provided by the principal investigator(s), federal government, and/or industry sponsors.
- Communicates with study sponsors, federal agencies, principal investigators, and sub-investigators about research projects.
- Provides resources for staff, patients, families. and community regarding research.
- Travels to clinical research sites, hospitals, physician offices, and facilities within the System as necessary.
- Performs other duties as assigned within department
Benefits
- comprehensive suite of Total Rewards: benefits and well-being programs
- competitive compensation
- generous retirement offerings
- programs that invest in your career development
- 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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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
1-10 employees
