Career Opportunities

This position works within the Clinical Research Administration Office (CRAO) and in collaboration with the Colorado Clinical Translational Science Institute. CRAO is seeking a full-time clinical trials Calendar Builder at the Anschutz Medical Campus. As a key member of the finance and clinical research support team, this position works extensively with budget specialists, clinical research coordinators, principal investigators, various stakeholders of the University of Colorado Cancer Center, University and University of Colorado affiliates, to assist with building of calendars in accordance with budgets in the OnCore Clinical Trials Management System (CTMS). This position will be responsible for the ongoing support of the calendar and budget build functions in OnCore.

The OnCore Application Coordinator is a position within the University of Colorado Clinical Research Administration Office. As a key member of the application support team, this position encompasses a wide variety of duties and responsibilities. This individual works extensively with professionals in all areas of the University, and UCD affiliates, to assist with the ongoing support of the Clinical Trial Management System (CTMS) used at the University of Colorado Denver | Anschutz Medical Campus. The OnCore Application Coordinator will provide support for all ongoing training needs, ranging from assisting with access to the training environment to grading training exercises and establishing accurate permissions for users. The OnCore Application Support Role will be part of the team with the Oncore trainers and system manager to assure that the UCD research community has access to the most up to date materials for training and ongoing use of Oncore, the CTMS.

Serves as Assistant Director of Clinical Research Administration for the Office of Clinical Research (OCR) reporting to the Director of the OCR, in coordination with the Director of the Division of Sponsored Programs in the UF Office of Research. The Assistant Director has day-to-day responsibility for carrying out the OCR function as it relates to applicable sponsored programs relating to human subjects research or “clinical research”, including Power of Attorney to execute proposals and awards with sponsors, CDA’s, Clinical Trial Agreements, and Master Agreements. The Assistant Director will act in accordance with the policies and procedures established by OCR and will ensure that those actions are coordinated with the Directors of OCR and Sponsored Programs and the Office of Technology Licensing (OTL) as it relates to matters of research policy and intellectual property policy, respectively. The Assistant Director is also responsible for providing guidance and training of the research administration teams with regard to clinical research administration trends and issues.

The University of Michigan Medical School Clinical Trials Support Office, a unit of the Medical School Office of Research, is seeking an experienced, dynamic professional to serve in a highly visible role as the (change) administrative lead for a new enterprise-wide clinical trials management system, OnCore. This individual will administrate and directly supervise designated OnCore support personnel and coordinate the system support.

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The Clinical Trials office at the Keck School of Medicine is seeking an OnCore Training and Operations Manager to join its clinical trials administration team.

This position serves as a primary point of contact for OnCore application support for all departments conducting clinical trials. This role is responsible for providing general subject matter expertise and training in the use of OnCore in the management of clinical trials. This position further is responsible for report writing, training, and end user support, as well as supervising administrative users within the Clinical Trials Office.

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