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% Design research-informed sessions and modules for program participants ? 20% Conduct in-person and online data collection (surveys, interviews, focus groups, and session observations) and desktop research
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able to work effectively with minimal supervision Computer skills required Preferred Qualifications Previous experience working in a research laboratory setting desirable Experience in grant application
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to prepare routine reports and correspondence. Ability to interpret and follow instructions in written, oral, diagrammatic or schedule form. Ability to define problems, collects data, establish facts and draw
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electrophoresis, and fluorescent scanning. Use new techniques to assist in research progress and perform statistical analysis of data. Prepare and perform internal progress reports on experiments. Attend weekly
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blood pressure monitoring; Track the collection of study data. Assist with REDCap database design, security, data storage and management; Engage with community members to disseminate study findings
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addition, Candidate will support research workers by assisting with aspects of participant visits including scheduling, collecting anthropometric data and biospecimens, as well as completing interviews
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maintenance of study data, ensuring adherence to study activities as described in the protocol, and working with other members of the research team to coordinate all other aspects related to the conduct
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participants, coordinate research visits, collect high-quality clinical and questionnaire data, and ensure successful execution of study activities. This position offers an outstanding opportunity
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compliance with protocol requirements and institutional policies. Supervise, train, and evaluate research data associates and student volunteers. Participate in clinical research and clinical trials, as
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complex information; collaborates and builds consensus among the GMP team members and users. May present at conferences and seminars. Participates in the development of funding proposals, manuscripts, and