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.