888 data-"https:" "https:" "https:" "https:" "https:" "https:" "SciLifeLab" "IFM" "IFM" positions at University of Colorado
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prohibited under these policies, and student disclosures of pregnancy or related conditions directly to the OIE and to provide OIE’s contact information to any student disclosing pregnancy or related
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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
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. · Consistent attention to detail. · Ability to communicate effectively, both in writing and orally. · Strong commitment to keeping confidential information, confidential. · Ability
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nationally. The Clinical Research Coordinator is responsible for participant recruiting, consenting, scheduling, performing study visits, processing lab samples, entering data and other study-related duties
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payroll distributions · Work with Department Administrators on Payroll distributions and PETs Assist PASS Core/PIs with other support (OS) and progress report (RPPR) information – 10% · Maintain
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or similar grant submission software. Experience with CU Data, A2E, HCM and CU Marketplace. Experience working in an academic environment or medical center. Experience with PeopleSoft (HRMS &/or Finance
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care practitioners, and members of the public expressing information needs. This Access Services Specialist will serve as the backup for opening operations for the library, including the physical
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communicate and present data to stakeholders Collaborate with Research Services Program Director and Research Administrative Team on various projects including helping monitor study coordinator time/utilization
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. Coordinate and schedule final grading meetings with faculty and liaise with the MD Data Records Manager and university registrar for grade entry. Clinical Site Badging and Credentialing- 10% Act as a point of
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current medication information, review the research protocol inclusion/exclusion criteria, and confirm the eligibility of the subject to participate in the clinical trial Perform the informed consent