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. Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies. Collect and manage patient and laboratory data for clinical research
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of proposals within parameters of sponsored research guidelines. Oversee and communicate submission process, both paper and electronic, review documents for completeness and compliance. Develop, prepare, and
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complex issues to other staff. Input data, update electronic databases, web sites, literature, and associated materials. May collect, gather and validate data, prepare basic reports. Coordinate logistics
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in study design and proposal development Create analytic files with detailed documentation. Prepare data for analysis by cleaning, identifying cohorts, reshaping data, creating new variables, merging
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and/or vision science Experience with Javascript, development of web apps and database architecture is a plus but not required Desire to work in a fast paced, collaborative team-science environment
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model APIs, cloud computing environments, and R for additional statistical analysis. For decision support prototype development and evaluation, web-based user interface design, human-computer interaction