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Henry Ford Hospital - Detroit, MI

posted 28 days ago

Full-time
Detroit, MI
Hospitals

About the position

Under minimal supervision, coordinates clinical research projects in compliance with the Code of Federal Regulations. Provide technical support to Principal Investigators. Analyze protocol specific requirements and implement quality assurance measures to ensure physician, patient and clinician compliance. Abstract medical information from various sources in the patient medical record. Report adverse events to medical monitor, FDA, and all other governing bodies. Coordinate all external audits and monitoring visits, and serve as liaison between institution and sponsor. Serve as departmental and system-wide resource.

Responsibilities

  • Coordinate clinical research projects in compliance with the Code of Federal Regulations.
  • Provide technical support to Principal Investigators.
  • Analyze protocol specific requirements and implement quality assurance measures.
  • Abstract medical information from various sources in the patient medical record.
  • Report adverse events to medical monitor, FDA, and all other governing bodies.
  • Coordinate all external audits and monitoring visits.
  • Serve as liaison between institution and sponsor.
  • Serve as departmental and system-wide resource.

Requirements

  • Bachelor's degree in Clinical Research, Biology, Chemistry, Nursing or other closely related field.
  • Two (2) years of relevant experience preferred.
  • Previous coordinator experience preferred.
  • Organizational and analytical and problem solving skills.
  • Demonstrated verbal and written skills at professional level.

Nice-to-haves

  • SOCRA or ACRP and IATA certification preferred.
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