856 data-"https:" "https:" "https:" "https:" "https:" "https:" "SciLifeLab" "IFM" "IFM" positions at University of Colorado
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both a project manager and a program navigator, functioning as the central operational and coordination hub for ASCEND activities and fulfilling data and reporting requirements. The nature of this work
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assessments and study interviews. Responsible for data management for all clinical trial data. Collect, code, and analyze data obtained from research in an accurate and timely manner. Reviews and resolves data
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the Hopfer Lab (PI: Christian Hopfer, MD). The primary focus of the Hopfer Lab clinical research coordinator will be assisting with data collection on a clinical trial in the Rocky Mountain Cannabis Research
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#: 00816489 – Requisition #: 38647 Job Summary: The Colorado Center for Personalized Medicine (CCPM) at the University of Colorado Anschutz Medical Campus advances the use of genetic information to guide care
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Responsibilities: Incentive Plan Administration (50%): This position is responsible for implementing and administering the Department’s four incentive plans, which includes data collection, calculation, and payment
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ACGME accreditation requirements. Finance: Tracks budget items and fellow funding based on information provided by Business Manager and Program Director(s). Processes fellow expenses in the appropriate
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the C3 Lab that involve: working closely with a research team domestically and internationally, data organization and quality, data collection instrument development and maintenance, data description
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technical research activities, laboratory functions, data entry and oversight using electronic systems, and ensuring compliance with reporting requirements for protocols and projects. Key Responsibilities
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, documents, databases, and related materials and information. Provide support researching issues and developing recommendations to resolve process, unit and related issues. Assist in the review and
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-Initiated Clinical Trials. This position focuses primarily on the responsibility of data collection, interpretation and documentation of clinical research data, and meeting with research patients for study