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Henry Ford Health in Detroit is seeking a Research Study Coordinator II to manage and coordinate clinical research projects under regulatory guidelines. You will support Principal Investigators and oversee day-to-day study operations.
The role involves direct contact with potential and enrolled participants, interaction with internal and external stakeholders, and multi-study coordination, ensuring compliance and timely study progress.
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.
Qualifications
Bachelor's degree in a scientific field, Psychology, Sociology, Anthropology, or related field.
One (1) year of research project coordination experience.
SOCRA or
ACRP and IATA certification preferred.