Responsible for implementing clinical research activities within the Cardiovascular Division with locations at HUP and PPMC. Responsible for assisting with study coordination and recruitment for industry sponsored studies. Works directly with study physicians, research directors, and other research staff. Major duties include screen/enroll patients, conduct follow-up assessments, data collection and use of EDC systems, and assessment of adverse events. This coordinator will assist in ensuring patient and data safety, manage samples and related processing, and will be a proactive communicator with the team and its PIs. Organize and coordinate study procedures, schedule study visits within protocol designated time frames, assure research orders are properly entered into the electronic medical record. Follow-up telephone calls/interview, conduct study visits, including administering questionnaires, escorting patients to protocol-required tests and procedures. Create Smart phrases in EPIC/Penn Chart. This position is contingent upon favorale funding.
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Job Type
Full-time
Career Level
Entry Level
Number of Employees
11-50 employees