Research Study Coordinator I - Cancer Clinical & Trans Research - 40 hours - Days

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.

EDUCATION/EXPERIENCE REQUIRED:

• Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology or related field.

• CERTIFICATIONS/LI

• CENSURES REQUIRED: SOCRA or ACRP and IATA certification preferred.

• Preferred Skills

• Research Experience

• Good Communication skills

• Reliable transportation to drive to various locations,

• Clinical skills including phlebotomy could be extremely useful but not required.

Additional Information

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