806 evolution "https:" "https:" "https:" "https:" "https:" "https:" "UCL" "UCL" "UCL" "UCL" positions at University of Colorado in United States
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. This role provides a strong foundation for professional development, with opportunities to gain valuable experience in a fast-paced academic healthcare environment. Key Responsibilities: Instrument and
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Calculator: http://www.cu.edu/node/153125 The salary of the finalist(s) selected for this role will be set based on a variety of factors, including but not limited to, internal equity, experience, education
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contributions that add to your bottom line. Benefits statement to include in all benefits-eligible positions. See Eligibility Matrix. Benefits: https://www.cu.edu/employee-services/benefits Total Compensation
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website: https://medschool.cuanschutz.edu/accords. The successful candidate will assist with study and instrument design and data coordination, conduct data cleaning and analysis of primary and/or secondary
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, microscopy, sequencing). Collaborate with a multidisciplinary team of investigators, clinicians, and trainees. Contribute to publications, presentations, and grant development. Prepare and submit grant
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-2028 reviews to the next cycle. Policy Coordination Provide supervision and oversight of the policy development process, coordinating with Legal and others as appropriate. Colorado Department of Higher
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patient-oriented research or research conducted with human subjects. Patient-oriented research includes mechanisms of human disease, therapeutic interventions, clinical trials, or development of new
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Coordinator Position #: 00756542 – Requisition #: 38723 Job Summary: This position will participate as a member of the Cancer Center’s Oncology Clinical Research Support Team (OCRST) in the development and
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additional perks & programs with the CU Advantage . To see what benefits are available, please visit: https://www.cu.edu/employee-services/benefits-wellness Qualifications: Minimum Qualifications: Auditor
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), Western IRB (WIRB), and other regulatory agencies. This includes protocol development, writing consent forms, adverse event reporting, monitoring FDA-IDE trials, and managing continuing reviews of protocols