Senior Neuromodulation Clinical Trials Coordinator

Commonwealth of VA Careers

Charlottesville (VA)

On-site

USD 68,000 - 78,000

Full time

14 days+
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Job summary

University of Virginia's Center for Neuromodulation Research in Charlottesville, VA seeks a Clinical Research Coordinator to lead day-to-day operations across trials on non-invasive neuromodulation, including focused ultrasound and VNS, for substance use disorders and behavioral addictions.

You will recruit, screen, enroll, and retain participants; ensure protocol fidelity and regulatory compliance; manage data across REDCap; supervise junior staff; and conduct off-site visits at treatment

Qualifications

  • Bachelor's degree required or equivalent experience.
  • Minimum 3 years clinical research experience; Master’s may substitute.
  • CCRC/CCRP preferred; certification within one year.
  • Experience with substance use / psychiatric populations is advantageous.
  • Familiar with GCP, HIPAA, IRB processes.

Responsibilities

  • Screen and identify eligible participants and maintain enrollment logs.
  • Obtain informed consent per IRB procedures and explain risks.
  • Coordinate off-site recruitment and study visits at treatment centers.
  • Manage data entry and REDCap databases; ensure data quality.
  • Support regulatory submissions, monitoring visits, and audits.
  • Train staff and contribute to SOPs and manuscripts.

Skills

Strong organizational skills
Excellent interpersonal and written/or

Education

Bachelor's degree
Master’s degree may substitute
CCRC/CCRP preferred
Degree in health, life sciences, psychology, neuroscience

Tools

REDCap
IRB submissions familiarity
R / SPSS / MATLAB / Python

Job description

University of Virginia's Center for Neuromodulation Research in Charlottesville, VA seeks a Clinical Research Coordinator to lead day-to-day operations across trials on non-invasive neuromodulation, including focused ultrasound and VNS, for substance use disorders and behavioral addictions.

You will recruit, screen, enroll, and retain participants; ensure protocol fidelity and regulatory compliance; manage data across REDCap; supervise junior staff; and conduct off-site visits at treatment

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