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Clinical Study Coordinator

4 months ago

Detroit, United States Henry Ford Hospital Full time

GENERAL SUMMARY:

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.

EDUCATION/EXPERIENCE REQUIRED:

* 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.

CERTIFICATIONS/LICENSURES REQUIRED:

* SOCRA or ACRP and IATA certification preferred.

Additional Information

* Organization: Henry Ford Medical Group
* Department: Cancer Clinical & Trans Resear
* Shift: Day Job
* Union Code: Not Applicable