Research Study Coordinator III - Cancer Clinical & Trans Research - Full Time

GENERAL SUMMARY:

Under minimal supervision, coordinates research projects within guides of regulatory compliance and/or Code of Federal Regulation. Provides technical support to Principal Investigators. Duties include but not limited to, interacting with both internal and external customers at all levels and oversight of recruitment and coordinating day-to-day operations of the study. Direct contact with potential and enrolled study participants expected. Provides other support as required. May work on multiple studies at any given time.

EDUCATION/EXPERIENCE REQUIRED:

• Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology, or related field.
• Three (3) years of relevant experience with at least two (2) years of research project coordination experience.

CERTIFICATIONS/LICENSURES REQUIRED: SOCRA or ACRP and IATA certification required.

Additional Information

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