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, along with any corresponding amendments. Liaises between external sponsors and COH departments to determine suitable coverage justifications and cost allocations for unique clinical trial procedures. As
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’ specimen and data collection activities. Maintain a system for effective study management and tracking of data and specimen collection. Serve as a resource for CRAs and/or Phlebotomists, and as a liaison
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independently. Our resource rich environment enables research from basic science to the development of clinical trials. Innovation and Techniques : Our lab consists of a diverse group of scientists and clinicians
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clinical trial. The Clinical Trials Manager will be responsible for managing the volume of the studies under his/her purview and working with the portfolio supervisor to resource research staff to each study
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edge tools/resources relevant to writing and graphical design, video editing, plagiarism detection, journal selection, etc. Your qualifications should include: · Requires a PhD in integrative
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in exercise physiology and research methodology. Resource & Workflow Management: Assesses staffing needs, schedules work activities, and ensures efficient coverage and service delivery. Your
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cancer prevention and control education; increase awareness and utilization of resources; and increase community participation in health and biomedical research. Our model is a community participatory
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current on literature in the field and cutting edge tools/resources relevant to writing and graphical design, video editing, plagiarism detection, journal selection, etc. Your qualifications should include
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working relationships and communicates effectively and positively with research and Animal Resources Center staff. Your qualifications should include: High School or equivalent. Preferred qualifications
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analysis plans, assist in software development, and serve as a resource for divisional statisticians and staff. As a successful candidate, you will: Collaborates on research projects, assisting with