How to Apply
A cover letter is required for consideration for this position and should be attached as the first page of your resume. The cover letter should address your specific interest in the position and outline skills and experience that directly relate to this position.
As part of the strategic research initiative, the Clinical Trials Support Office is now overseeing a new model to improve clinical care, value, and health outcomes by successfully executing a diverse portfolio of high-quality clinical trials. This new model entails an organizational structure of local service units, central infrastructure, and governance oversight. The Clinical Trials Support Units (CTSUs) are trans-departmental and thematically aligned based on research foci. CTSUs are the local units that provide comprehensive pre- and post-award support to study teams, offering high-quality, efficient service in support of a mix of clinical trials.
The Research Process Coordinator will be responsible for pre- and/or post-award research administration activities for the Behavior, Function & Pain and Children’s CTSUs, with a current specific emphasis on post-award support of federally funded trials.
Handle post-award activities ensuring all Medical School, University, and sponsor policies and guidelines are followed. Specific duties include account reconciliation, processing patient reimbursement, invoicing sponsors, resolving clinical research billing errors, ensuring revenue collection, and handling uniform guidance (A-21) reports and Financial Status Reports. Provide assistance in completion of progress and final reports as applicable. While not planned initially, specific pre-award duties may include UFA, CTRF, and PAF creation and routing, and budget creation and negotiation.
Build and foster relationships with other units, as well as sponsors. Serve as liaison for faculty with sponsor, and University central offices (i.e. Sponsored Programs and ORSP). This will require close collaboration and frequent communication with departments, faculty, study teams, research administrators, and others.
Other duties and special projects as assigned.
Bachelor’s degree or equivalent experience with 2-5 years of experience specifically in finance, management, business, or a related field.
Experience with pre- and/or post-award research administration activities, preferably clinical trials.
Solid understanding of sponsored projects, particularly the aspects of clinical research finances and reporting requirements.
Ability to work independently with minimal supervision and with diverse teams of people in a diplomatic, collaborative, and effective manner.
Excellent interpersonal, oral, and written communication skills with exceptional attention to detail.
Excellent computer skills including proficiency in finance related programs/tools such as Excel, M-Pathways, M-Reports, and the Data Warehouse.
Ability to manage multiple tasks simultaneously, to work well under time constraints, and meet deadlines, as well as prioritize and exercise good judgment.
Understanding of some basic medical terminology.
Demonstrated experience working with a variety of sponsors including industry, federal agencies, cooperative groups, foundations, and gifts.
Experience with the U-M systems including MBECT and HSIP.
Knowledge of Medical School and/or University policies and procedures.
Michigan Medicine conducts background screening and pre-employment drug testing on job candidates upon acceptance of a contingent job offer and may use a third party administrator to conduct background screenings. Background screenings are performed in compliance with the Fair Credit Report Act.
Job openings are posted for a minimum of seven calendar days. This job may be removed from posting boards and filled anytime after the minimum posting period has ended.
U-M EEO/AA Statement
The University of Michigan is an equal opportunity/affirmative action employer.