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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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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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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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those patients faced with limited options. A hallmark of TGen is our belief that by utilizing the latest technologies and collaborating with the strongest of partners, we can develop better tools
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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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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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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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substitute for minimum education requirements. · 3-5 years of experience with a Bachelor’s or 0-4 years of experience with a Masters · Basic biology and chemistry experience
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of work performed, including results and methodology; utilizing records may calculate, graph, and compile data. Develop techniques and expertise in one or more areas relevant to laboratory research projects