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Clinical Study Coordinator- Cancer Clinical and Translational Research Office -
Detroit, MI
Job Description
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
Equal Employment Opportunity/Affirmative Action Employer
Equal Employment Opportunity / Affirmative Action Employer Henry Ford Health System is committed to the hiring, advancement and fair treatment of all individuals without regard to race, color, creed, religion, age, sex, national origin, disability, veteran status, size, height, weight, marital status, family status, gender identity, sexual orientation, and genetic information, or any other protected status in accordance with applicable federal and state laws.
Job Summary
Company
Start Date
As soon as possible
Employment Term and Type
Regular, Full Time
Required Education
Bachelor's Degree
Required Experience
2 years
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