Research Study Coordinator I- Full time- Electrophysiology Research
Henry Ford Health, Detroit, MI, United States
Overview
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.
Responsibilities
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/LICENSURES REQUIRED: SOCRA or ACRP and IATA certification preferred.
1-2 yrs of previous experience in clinical trials
Preferred background with Cardiology
Preferred experience as MA (blood draws, lab processing, charting, etc)
Organization and Department
Organization: Henry Ford Medical Group
Department: Cardiovascular Medicine
Shift: Day Job
Union Code: Not Applicable
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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.
Responsibilities
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/LICENSURES REQUIRED: SOCRA or ACRP and IATA certification preferred.
1-2 yrs of previous experience in clinical trials
Preferred background with Cardiology
Preferred experience as MA (blood draws, lab processing, charting, etc)
Organization and Department
Organization: Henry Ford Medical Group
Department: Cardiovascular Medicine
Shift: Day Job
Union Code: Not Applicable
#J-18808-Ljbffr