Oncology Clinical Research Coordinator

Patient Recruitment and Scheduling. Identifies, recruits, and schedules patients who may be eligible to participate in the oncology clinical research program.Assessment. Performs the initial assessment of potential patient participants, including but not limited to taking detailed clinical history, performing physical exam, and completing patient data forms.Testing and Training. Conducts research tests and supervises exercise training sessions.Information Distribution. Provides potential patient participants with study information. Obtains informed consent forms.Clinical Resource. Acts as the initial clinical resource and liaison between physicians, nurses, and laboratory personnel.Data Management. Responsible for data management and data analysis. Ensures data entry is accurate and completed in a timely manner.FollowUp. Responsible for the initiation, organization, and handling of patient followup. Assesses and analyzes patient monitor data at all followup visits. May oversee the conduct of homebased patient training programs.Meeting Attendance. May attend various meetings pertaining to the oncology clinical research program. May present information at the meeting.Personnel Supervision. Assumes lead role to ensure adherence to protocol. Directs and evaluates the work of research personnel. Trains and schedules workloads of employees.As Needed. Performs various duties as needed to successfully fulfill the function of the position.

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