Clinical Research Coordinator (CRC) - (Eugene, OR)

Description Supports enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol qualifications. Responsible for working with the principal investigator to meet or exceed study enrollment. Reviews the study design and inclusion/exclusion criteria with physician and patient. Ensures the protection of study patients by verifying informed consent procedures and adheres to protocol qualifications/compliance. Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review. Monitors data for missing or implausible data. Ensures that adequate and accurate records are maintained for inspecting. Creates study specific tools for source documentation when not provided by sponsor. Collects, completes, and enters data into study specific case report forms or electronic data capture systems. Generates and tracks drug shipments and supplies as needed.