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the computer tracking system building in appropriate safety checks. Creation of source documents and Case Report Forms as directed by the data manager utilizing established SOP and an existing computer design
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support: Assist with scheduling, user engagement, and tracking project activities Support recruitment and consenting of study participants under supervision Review clinical and patient records to support
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relate to ongoing research in the lab. Field Work: Assist with field-work as needed. Lab supplies: Assist in ordering; keeping track of supply inventory; unpacking lab supplies and putting them in proper
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). This position supports multiple key university graduate administrative services in FASS including: development of processes, application and admissions, student registration, records and progress tracking, degree
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patients who are eligible to participate in the study. Designs, creates and maintains research database for clinical trials. Tracks the status of research trials into database. Assists with drafting
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Hospital. Responsibilities include development and completion of the Case Report Forms (CRF’s), electronic data entry and database management, and tracking enrolled subjects for long-term follow-up
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goggles). Consequence of Error/Judgement Errors in tracking aspects of the project, data recording and entry, or breaches in confidentiality have the potential to negatively impact research projects
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. The candidate will be primarily responsible for participant recruitment, schedules, data collection, data tracking, data entry, and data checking under the direct supervision of Dr. Teresa Liu-Ambrose and will
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updates verbally and in written form to management, as needed Complete any necessary administrative tasks such as time tracking Demonstrate commitment to client’s needs and confidentiality Education and
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quantitation of gene expression 4) Maintaining solutions (keeping track and maintaining consumables and reagent stocks and lab inventories) and other general lab maintenance. 5) Analysis of results and