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Proven ability to find creative and innovative solutions to adjusting needs of the center. Strong experience completing clinical trials case report forms via hard copy and online. Strong knowledge of investigational protocols especially with colorectal surgery protocols (data management, query resolution, protocol design, protocol writing, and protocol implementation).ĭemonstrated experience with research protocol in order to screen patients for eligibility, initiate treatment plan, collect specimens, and orient participating physicians. Strong knowledge of investigational protocols (data management, query resolution, protocol design, and protocol implementation).ĭemonstrated experience performing clinical research duties in a clinical research environment such as CRO, academic research institution, and/or a research hospital.Įxperience in providing work direction and assisting supervisor in maintaining an efficient medical research team.

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Strong experience in clinical trials research including budget negotiations and invoicing per clinical trial agreement. Strong knowledge of experimental protocols, data gathering, protocol design, and evaluation.ĭemonstrated experience in research protocol start-up procedures, including: study feasibility, study activation and IRB processes, and qualification procedures. Strong theoretical knowledge and/or Bachelor's Degree in a social science or basic science such as Biology, Microbiology or a related field and/or an equivalent combination of education and work experience.ĭemonstrated experience in clinical trials research. Work closely with federal and state regulatory officials. Independently create original documents and policies for assigned disease teams. Assist PIs with proposals, progress reports and manuscripts. Provide education and information to the general public concerning the ongoing clinical trials.

Provide direction and guidance to investigators. Oversee the quality of the medical and clinical research data. Assure compliance with state and federal regulatory guidelines. The Clinical Research Coordinator 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. Create informational and recruitment materials and act as a liaison with other UCSD departments and agencies for the purpose of implementation of studies. Incumbent will coordinate and oversee start-up procedures, implementation, recruitment, screening, enrollment, and maintenance of subjects. UC San Diego Health is currently ranked among America's best hospitals by U.S. The missions of research, education and patient care are intertwined, and are integral to the goals of the department.Īs a leader in research and patient care, the UC San Diego Department of Surgery is committed to providing the latest in expert and compassionate treatment, performing leading-edge research, and training the next generation of top surgeons and scientists. Annual expenditures across the Department total over $66.5M with a global research portfolio of over $19M. Activities are organized in 13 sub-specialty divisions.

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The Department of Surgery is one of the largest departments in the School of Medicine and is comprised of 102 full time faculty members, 220 voluntary faculty members, 20 physicians employed on MSP agreements, 25 doctors employed by the VA or other facilities, 77 accredited and 13 non-accredited trainees and 100 career staff. This position will work a hybrid schedule which includes a combination of working both onsite on Campus and remote.