Overview
GENERAL SUMMARY : Under limited supervision, carries out research projects within guides of regulatory compliance and / or Code of Federal Regulation.
Duties include but are not limited to interacting with both internal and external customers at all levels and completing day to day operational tasks for the study.
Direct contact with potential and enrolled study participants expected.
May analyze protocol specific requirements and implement measures to ensure stakeholder compliance.
Provides other support as required.
Responsibilities
- Under limited supervision, carries out research projects within guides of regulatory compliance and / or Code of Federal Regulation.
- Duties include but are not limited to interacting with both internal and external customers at all levels and completing day to day operational tasks for the study.
- Direct contact with potential and enrolled study participants expected.
- May analyze protocol specific requirements and implement measures to ensure stakeholder compliance.
- Provides other support as required.
Education / Experience Required
High School Diploma or G.E.D. equivalent.Three (3) years of work experience, with a minimum of two (2) years research and / or healthcare experience.ORAssociates degree in a research or healthcare related field.One (1) year of research and / or healthcare experience.Additional Information
Organization : Henry Ford Medical GroupDepartment : Research Design and AnalysisShift : Day JobUnion Code : Not ApplicableJ-18808-Ljbffr