This position assists in the coordination of various research projects and supports the Principal Investigator and other Clinical Research support staff in the acquisition of specimens and extraction of data from patient charts. This position also provides administrative/regulatory support by assisting with patient recruitment; scheduling study participants; providing operational support for the implementation and delivery of research studies; maintaining complete and accurate data and source documentation; and processing IRB and other regulatory documents as needed in accordance with federal, state, and regulatory agency and local requirements.
Associate's Degree or equivalent combination of education and experience (Required)
Bachelors Degree or related field (Preferred)
One year research experience or academic equivalent (Required)
ACRP or SOCRA Clinical Research Certification (Preferred)
Clinical Research Training Certification (Preferred)