Clinical Research Coordinator
Current-Prescreened clinic lists to identify eligible patients using protocol specific inclusion and exclusion criteria for participation in the Quebec Pancreas Cancer Study (QPCS) and its affiliate studies, documenting each potential participant's eligibility or exclusion -Approached and enrolled eligible patients into the QPCS and its affiliate studies.-Navigated patients through genetic testing and study participation requirements by scheduling and coordinating clinical research appointments, genetic testing and biospecimen collections as required by the protocol -Completed participant enrolment by 1) obtaining authorization for medical records as well as access to archived biospecimens and 2) sending requests for medical records and/or archival biospecimen acquisitions-Collected and performed data entry and management of online study databases-Prepared other study materials as requested by the PI. These study materials include, but are not limited to informed consent documents, case report forms (CRFs), screening and enrollment logs, and SOPs-Establish and organize study files, including but not limited to, regulatory binders, study specific source documentation and other materials-Assisted with returning of genetic testing results to patients and treating physicians