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, enrolls, and coordinates care of subjects in compliance with protocol requirements. The Clinical Study Coordinator may provide education on investigational agents/devices to research subjects and maintains
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document participant eligibility, safety, and protocol adherence, and report adverse events promptly. Pursue continuous education and training opportunities, staying updated with the latest clinical research
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various clinicians and researchers to coordinate biospecimens and informatics. · Develop systematic databases with members on campus. · PhD or MD degree in life or biomedical sciences, or a
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identification cards, and insurance cards. Prepares for upcoming registration appointments. JOB QUALIFICATIONS Experience Two years’ experience with healthcare admission and registration processes Education High
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to the Associate Director (AD). The COE's primary goal is to develop and lead the Cancer Center in facilitating catchment area community-engaged research and programs. This includes maintaining
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according to career stage and will help determine the rank of appointment (assistant, associate, or full professor): Scholarly accomplishments Extramural funding experience Impactful mentoring and teaching
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qualifications should include: Bachelor’s degree. Experience may substitute for minimum education requirements. (Associate Degree plus minimum of 2 years of experience). At least one year of experience related
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guidelines, and HIPAA regulations. Become familiar with institutional policy and procedures regarding conducting multiple clinical research trials. Develop and maintain knowledge of institutional protocol
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development and quality control (QC) activities to ensure GMP compliance for CBM products. Recruit, manage, and train QC staff for tasks in a cGMP facility. Review, revise, and develop standard operating
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experience or combined education and experience in related field. City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity, and inclusion, please click here