826 data-"https:" "https:" "https:" "https:" "https:" "https:" "Here We Are" positions at University of Colorado
Sort by
Refine Your Search
-
Listed
-
Category
-
Program
-
Field
-
experimental planning, assay development, and active participation in data interpretation and research advancement. Key Responsibilities: Perform basic molecular biology techniques, including buffer preparation
-
, information systems, or a directly related field from an accredited institution. Senior: 2 years of professional level experience in an academic, health care, or business related-environment Principal: 3 years
-
Parking at our 1800 Grant Street Office. Many additional perks & programs with the CU Advantage . Additional taxable fringe benefits may be available. For more information on benefits programs, please
-
information Proficiency in MS Office and Adobe software, including Word, Excel, PowerPoint, Illustrator, and Photoshop Ability to maintain a laboratory notebook Able to take the initiative to address research
-
the patients served; the ability to assess data reflective of the patient’s status and interpret the appropriate information needed to identify each patient’s requirements relative to their age-specific needs
-
resources, including navigating to policies, procedures, forms, learning resources, tax and other information • Investigates issues, identifying when action is required by other resources, and escalating
-
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
-
. · Consistent attention to detail. · Ability to communicate effectively, both in writing and orally. · Strong commitment to keeping confidential information, confidential. · Ability
-
stakeholders. Ability to independently recognize learning opportunities, design and conduct research, gather data, structure quantitative and qualitative analyses, and draw and apply actionable recommendations
-
, including accurate and timely CROMS data entry and ClinicalTrials.gov registration and results reporting, with alignment across reporting platforms. Provide study support and quality assurance, including pre