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The opportunity
The Screening Coordinator is responsible for providing participants with knowledge to make an informed decision regarding participation in an investigational trial and maintaining related knowledge and documentation. This position serves as an integral member of the site, clinical research and screening teams. 
How you’ll spend your day
Performs informed consent procedures according to the ethical standards expressed in the Declaration of Helsinki, and facilitates screening processes in strict compliance with  study protocols, standards of Good Clinical Practice, Standard Operating Procedures (SOP’s), QA/QC procedures, OSHA guidelines, Internal Review Board (IRB) approved Informed Consent Forms (ICFs) and other state and local regulations where applicable
Ensures the well-being and safety of participants complying with FDA and HIPPA regulations
Performs and/or participates in medical history collection/documentation, informed consent (ICF) and protocol reviews, assists with screening physicals and medical screening procedures
Prepares and maintains compliant study charts and documentation