Protocol Development Coordinator - Clinical Protocol Development
Thanks for your interest in the Protocol Development Coordinator - Clinical Protocol Development position.
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Basic education, experience and skills required for consideration:
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Master’s degree or in lieu of a master’s degree, a bachelor’s degree with a minimum of 3 years of relevant experience.
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Must have at least 1 or more years of relevant experience. Relevant experience must include at least one of the following:
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Development and/or use of research protocols (animal protocols, clinical research studies, or clinical trials)
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Writing of research protocols and/or grants
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Must have knowledge of:
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Clinical protocol review and approval process
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Basic biology
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Research study/experimental design
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Must have knowledge of Microsoft Word, Excel, and PowerPoint, Adobe Acrobat, Endnote or other reference manager.
Preferred education, experience and skills:
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Doctorate in biology, biochemistry, or other life science is preferred.
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Experience writing clinical trial protocols.
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Coursework or working familiarity of the following: immunology, physiology, oncology, endocrinology, genetics, epidemiology, biostatistics.
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Experience with development, implementation or execution of investigator-initiated pharmaceutical-funded studies or multi-center trials.
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Familiarity with federal regulations and guidelines pertaining to interventional and non-interventional clinical research, including IND applications.
City of Hope is committed to creating a diverse environment and is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, or status as a qualified individual with disability.
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