Philadelphia, PA9 days ago
This position will have the following responsibilities: 1) Assist research coordinators with study tasks, including assessing eligibility of potential subjects through methods such as screening interviews, review of medical records, and/or discussions with physicians and research staff, scheduling subjects for appointments and procedures as required by study protocols, conducting reminder calls and/or emails prior to study visits; 2) Assist with program-wide biospecimen management: collect, log, and ship samples according to study protocols, prepare sample collection kits, maintain inventory of lab supplies; 3) Support the Breast Cancer Clinical Trails Navigation Program: monitor program email and EPIC pool for referrals, communicate with patients to complete intakes and disclosure forms, match patients to clinical trials based on review of prior records, and route patients to designated trial teams; 4) Collect data per study protocol and SOPs. The primary role of the Clinical Research Assistant is to assist with study coordination and biospecimen management for breast cancer investigator-initiated studies, multi-center research studies, and patient-oriented clinical and translational research projects within the 2-PREVENT Breast Cancer Translational Center of Excellence (TCE).