Research Coordinator — Participant Tracking & Data

Medical University of South Carolina

Town of Charleston (NY)

On-site

USD 52,272,000 - 67,869,000

Full time

14 days+
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Job summary

Medical University of South Carolina seeks a Research Coordinator to oversee recruitment, screening, enrollment, and data collection for psychiatric studies. The role includes maintaining regulatory documents and assisting with audits, grant proposals, and dissemination of findings.

Requirements include a relevant bachelor’s degree or equivalent experience, familiarity with psychometrics, and ability to manage electronic/paper records with strict attention to detail.

Qualifications

  • Bachelor’s degree preferred in a relevant field.
  • Experience with federally funded studies or pharmaceutical trials preferred.
  • Experience with psychometric instruments required.
  • Ability to interpret and apply laws, regulations, policies and procedures.

Responsibilities

  • Coordinate and manage tracking of all research participants, including recruitment, screening, scheduling, enrolling, completion of visits, and reimbursement.
  • Document participant data and manage electronic and paper files, including data entry.
  • Collect routine clinical psychometric assessments and manage electronic and paper files, including data entry.
  • Maintain regulatory documentation as required by IRB and Good Clinical Practice Guidelines.
  • Scrutinize study procedures and suggest changes to procedures as needed.
  • Maintain research supplies and equipment.
  • Conduct study visits after hours to accommodate participants.
  • Perform other duties as assigned.

Skills

Regulatory knowledge
Psychometrics
Info systems
Written & verbal comms
Independent judgement
Team collaboration
Clinical trials
Time management

Education

Bachelor’s degree in psychology, neuroscience, biology or social science or quantitative field
High school diploma + 3 years relevant experience

Job description

Medical University of South Carolina seeks a Research Coordinator to oversee recruitment, screening, enrollment, and data collection for psychiatric studies. The role includes maintaining regulatory documents and assisting with audits, grant proposals, and dissemination of findings.

Requirements include a relevant bachelor’s degree or equivalent experience, familiarity with psychometrics, and ability to manage electronic/paper records with strict attention to detail.

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