Assist in providing day-to-day supervision of the clinical research projects ensuring research quality, regulatory compliance, and optimal support of ongoing studies.
January 21, 2020
Completed degree(s) from an accredited institution that are above the minimum education requirement may be substituted for experience on a year for year basis.
January 12, 2020
Provide comprehensive study coordination for University Transplant Biorepository including consenting, specimen collection, processing and dispersal processes in accordance with best practices of the project.
January 08, 2020
Participates in a variety of professional development programs to ensure understanding of most current methodologies, practices, and philosophies as applied to the relevant patient population and research area.
December 31, 2019
Plan and coordinate the initiation of research study protocol, and the implementation of operating policies and procedures.
December 26, 2019
Prepares progress reports to sponsors, assists with pre- and post- award grants administration including development, preparation, and writing of non-scientific narratives and scopes of work.
December 19, 2019
Reviews all regulatory requirements to ensure implementation of appropriate methods, practices, and procedures for all research activities in designated area.
December 10, 2019
Demonstrated ability to work with multiple constituents on a variety of projects, flexibility, and willingness to take on assignments are essential.
November 20, 2019
Tracking, renewal, and upkeep of all human subjects and non-human subjects research protocols.
October 07, 2019
Manage all aspects of Institutional Review Board (IRB) processes including new proposal submissions, amendments, project renewals, and ongoing communication.
September 19, 2019