Research Coordinator - Atrium Health Greater Charlotte Market
About The Position
Are you passionate about making a real difference in patients’ lives? As a Clinical Research Coordinator on our Trauma & Acute Care Surgery Research team, you’ll be at the forefront of groundbreaking studies that shape the future of critical care. Every day, your work will directly impact the care of critically ill and injured patients, helping advance treatments and improve outcomes for some of the most vulnerable populations. Why You’ll Love This Role Meaningful Work: You’ll contribute to research that saves lives and sets new standards in trauma and acute care medicine. Dynamic Environment: Experience nearly every part of the Carolinas Medical Center hospital system—from the Emergency Department and Operating Rooms to ICUs and inpatient units. Collaborative Team: Work alongside a 10-person Research team, Trauma and Acute Care Surgeons, APPs, and clinicians from multiple specialties in a supportive, team-driven environment. Cutting-Edge Research: Be part of approximately 15 active clinical trials at any given time, including investigational drugs, medical devices, and innovative care practices. What to Expect This is a fast-paced, high-impact position. Many of our studies require time-sensitive screening and enrollment, so adaptability and strong organizational skills are key. Our team provides 24/7/365 coverage at the Charlotte campus, ensuring research excellence around the clock
Requirements
- Bachelor's Degree and research experience required.
- Strong communication and teamwork skills
- Ability to thrive in a fast-paced, high-acuity setting
- Prepared to take on leadership responsibilities as the Lead Coordinator for a high-priority, Department of Defense–funded Traumatic Brain Injury (TBI) study
Nice To Haves
- Master's Degree preferred.
- Phlebotomy certification or venipuncture skills preferred.
- BLS HCP certification from AHA preferred.
- Certification in clinical research (SoCRA, ACRP) preferred.
- Prior experience in clinical trials, especially drug and/or device studies, is strongly preferred
Responsibilities
- Determines protocol-related needs to conduct the trial and orders supplies and equipment.
- Recruits and screens potential patients and obtains informed consent.
- Assists in providing patient education and benefits and risks of participating in a clinical drug trial.
- Designs organizational tools and forms to facilitate accurate data collection and recordkeeping.
- Conducts in-service programs, summarizes study schedule to assist in understanding and implementing a protocol.
- Manages research funds.
- Schedules patient visits and laboratory and diagnostic test procedures.
- Coordinates drug shipments, storage, and accountability with pharmacy.
- Coordinates with Investigational Pharmacy for subjects to receive required drugs.
- Reviews trends, problems encountered, patient adverse events, and patient progress.
- Draws blood or collect other samples as needed and eligible.
Benefits
- 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
11-50 employees
