The Research Assistant will assist with research efforts focused on acute leukemia and other blood cancers, and also serve as a scribe for a busy leukemia and bone marrow transplant practice.  Assistant will be expected to attend clinic with the Attending Physician and act as scribe during clinic visits with patients.  Assistant will also help with research related tasks such as researching topics for upcoming scientific and professional meetings and presentations, helping to prepare PowerPoint slides for talks, and organizing and planning the schedule of a busy attending hematologist.  Will assist with preparation of case reports and case studies for medical journals, helping prepare the attending physician for academic presentations at national meetings, performing searches and reviews of the medical literature to help with clinical questions and research efforts in leukemia and other blood cancers. Under supervision, will assist with coordinating and supporting research projects which may include, but are not limited to, the following duties: assisting with maintaining research data; gathering tests/results, physicians’ notes, and outside medical records in order to extract patient data and record data in approved format for study purposes (e.g. case report forms, data summaries); assisting with follow-up requests for data as necessary and assure comprehensiveness of individual data records; assisting with analyzing statistical data and providing reports as requested by Principal Investigators.

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The Clinical Research Coordinator (CRC) II will coordinate and oversee start-up procedures, implementation, recruitment, screening, enrollment, and maintenance of subjects. Create informational and recruitment materials and act as a liaison with other UCSD departments and agencies for the purpose of implementation of studies. The Clinical Research Coordinator (CRC) II will plan, develop and implement start-up procedures for multiple phase I-III research studies in assigned disease team as well as lead, direct, and coordinator operational efforts. Assure compliance with state and federal regulatory guidelines. Oversee the quality of the medical and clinical research data. Provide direction and guidance to investigators. Provide education and information to the general public concerning the ongoing clinical trials. Assist PIs with proposals, progress reports and manuscripts. Independently create original documents and policies for assigned disease teams. Work closely with federal and state regulatory officials.

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