This position involves research responsibilities for multiple projects. Responsibilities will be carried out in coordination with study investigators and with the support and assistance of research staff. Responsibilities will include: assistance with coordination and implementation of studies at multiple sites; data collection, data entry, data tracking, and data cleaning; use of study databases; and assistance with monitoring of accrual and quality assurance. This position will involve patient recruitment; data collection from human subjects, the collection of biospecimens, and the performance of other research project-related tasks. The position will also involve the coordination of several drug clinical trials, in a primary role.
Benefit packages for this role will start on the 31st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.