The Research Study Assistant position will encompass preparation of study protocols and research study materials including recruitment material, case report forms
(CRFs), Institutional Review Board applications and documentation for clinical projects.
ESSENTIAL JOB FUNCTIONS:
Preparation of study protocol case report forms (CRFs)
Data collection on CRF forms in participant research file. Data entry into database for data analysis.
Preparation of documents for progress and final reportsof clinical research protocols for various entities including the funding entity (NIH or other), BUMC Institutional Review Board (IRB),GCRU/CTSI and others as deemed necessary
Maintaining participant research files during participation in the study protocol
Bachelors degree with one year of Experience