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, participant recruitment and retention, data collection and management, coordination across interdisciplinary teams, and engagement with community and institutional partners. The role supports the efficient
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analyze results, including analyses of archived data, while adhering to standard procedures and guidelines. This position will manage all animal projects in CAMIPM. Duties include but not limited to carry
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documentation of workflows and contribute to data quality control to ensure reproducibility. The candidate will also be required to read relevant scientific literature to for establishing new technologies and
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documentation- including source documentation, case report forms, and research charts. Collect, review and report study data, Complete case report forms and resolve data queries Participate in the initiation
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lab visits to assess CO, e-cigarette and cigarette use across 6 weeks; and (5) follow up with participants who reschedule or fail to show for an appointment, enter the study data, and ensure adequate
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samples; collecting and filing study documents; and collecting and entering clinical data. Utilizing a variety of electronic systems, the CRC will document study activities with accuracy. The coordinator
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computer-based systems. Flexibility, teamwork, and a sense of humor are valued attributes for success in this role. This is a year-round, part-time position offering a flexible schedule and the opportunity
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maintaining transgenic mouse lines that may include breeding, genotyping, keeping precise records, dissecting tissues and data collection/analysis. The candidate should be able to work independently as
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laboratory experience is preferred but not required. Proficiency with standard computer applications (e.g., Excel, Power Point, GraphPad, Adobe Photoshop and ImageJ analysis) is essential. The ideal candidate
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for all aspects of study coordination including subject recruitment, detailed data entry, collecting biospecimens, subject visits and follow-up and regulatory documentation. Job Description Job