Allentown, PA30+ days ago
This includes performing required study procedures as applicableApply knowledge and skills to independently review new protocols, consents, and other clinical trials documents to ensure protocol complianceReview and extract data from medical charts to screen patients for eligibility for assigned protocolsReview consent form, protocol procedures, and treatment regimen with potential patients and obtain consent from interested participants, documenting the consent process as requiredMaintenance of accurate and complete documentation, including but not limited to regulatory documents, signed informed consent forms, source documentation, drug dispensing logs, subjects logs and study-related communicationOrganizational management of all aspects of the trial including but not limited to timeliness in completing case report forms (CRFs), data entry, reporting adverse drug events, managing caseload and managing study filesObtain data from other departments (radiology, pathology, etc.) as required by each protocolPrepare research charts for monitoring visits and auditsRespond to data queries and collate data as requested by research group or investigator, and maintain quality source documentation PHYSICIAL AND SENSORY REQUIREMENTS: Requires sitting for up to seven hours per day, 4 hours at a time. Individually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care.