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support multiple externally funded investigator initiated and cooperative group clinical trials. The CRC will be responsible for patient screening, subject enrollment, scheduling, collecting, storing and
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and media studies. Ability to understand, analyze, and clearly communicate complex research ideas for multiple audiences. Excellent writing skills and experience in writing research and policy briefs
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. Candidate must demonstrate ability to prioritize and manage multiple projects; to write clearly and professional; to represent faculty and degree programs at recruitment activities; to effectively interact
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citizen rights, civic responsibility, democracy and the Constitution. Job Responsibilities Work with multiple stakeholders to manage and organize existing web content for the development of a new web
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. Significant experience is required in immunohistochemistry, detailed image analysis, and manuscript writing. . The applicant must be highly motivated, able to work on multiple projects simultaneously, and have
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who can manage multiple priorities and facilities and deliver high-quality programs and services. This position encourages developing new ideas, systems, and technologies, but also analyzing and
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multiple and complex databases, requiring advanced SAS skills and more experience in the effective manipulation of large data. Strong teamwork and collaboration skills are needed to support multiple projects
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the management of multiple clinical trials and will be responsible for study coordination for industry studies, investigator-initiated studies, and multi-center research studies. They will facilitate, promote and
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entry of patient visits and patient care for multiple trials and database projects. Job Description Responsibilities include: Coordinate the conduct of multiple clinical trials and registries. Screen
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visits and medical chart follow-up, biospecimen collection across multiple locations across the health system, biospecimen processing, and regulatory management. This position involves working directly