Psychiatry Clinical Research Coordinator

Ohio State University

Columbus (OH)

Vor Ort

USD 52.000 - 72.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

The Ohio State University’s Medicine | Psychiatry department seeks a Clinical Research Coordinator to coordinate daily clinical trials, recruit and consent patients, and manage study visits at Harding Hospital. The role requires IRB/FDA awareness and strong regulatory practices within a fast-paced clinical research setting.

Responsibilities include scheduling procedures, collecting data, and ensuring sponsor expectations are met, with emphasis on patient safety and accurate documentation.

Qualifikationen

  • Bachelor’s degree in biological/health sciences or related field.
  • 1 year of relevant experience required.
  • 2–4 years of relevant experience preferred.

Aufgaben

  • Coordinate and perform daily clinical research activities per trial protocol.
  • Recruit, interview and enroll patients and obtain informed consent.
  • Schedule patient appointments and study procedures.
  • Collect and document vital signs and biological samples.
  • Ensure regulatory compliance with IRB, FDA and sponsor requirements.
  • Prepare regulatory documents and assist with external reviews.
  • Attend departmental and investigator meetings.

Kenntnisse

Clinical research coordination
Patient recruitment
Informed consent
Data entry
Regulatory compliance
IRB/FDA knowledge
Study visits coordination
Vital signs collection
Surgery scheduling
Sponsor liaison

Ausbildung

Bachelor’s degree in Biological Sciences / Health Sciences / Social Sciences or related field

Jobbeschreibung

The Ohio State University’s Medicine | Psychiatry department seeks a Clinical Research Coordinator to coordinate daily clinical trials, recruit and consent patients, and manage study visits at Harding Hospital. The role requires IRB/FDA awareness and strong regulatory practices within a fast-paced clinical research setting.

Responsibilities include scheduling procedures, collecting data, and ensuring sponsor expectations are met, with emphasis on patient safety and accurate documentation.

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