Research Study Coordinator II - Clinical & Trans Research - 40 Hours - Days

GENERAL SUMMARY:

Under minimal supervision, the Research Study Coordinator II, is responsible for:

• 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.

• One (1) year of research project coordination experience.

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