Intermediate Clinical Sciences Professional
University of Colorado Anschutz Medical CampusAbout the role
Job Number:
37906)Description
University of Colorado Anschutz Medical Campus
Department of Pediatrics | Section of Neonatology
Job Title: Intermediate Clinical Sciences Professional
Position #: 00832133 – Requisition #:37906
Job Summary:
The Department of Pediatrics, Section of Neonatology, has an opening for a full-time Intermediate Clinical Sciences Professional for the Neonatal Outcomes Research Alliance (NORA) on the Anschutz Medical Campus. NORA is a collaborative of providers and clinical researchers in perinatal medicine within the Section of Neonatology. The successful candidate will actively participate in facilitating research and quality improvement projects conducted by NORA investigators. Research responsibilities will include enrolling study participants, administering study surveys, conducting interviews with study participants, and managing IRB applications and submissions. Project management responsibilities will include supporting the progress of Colorado hospitals' participation in various statewide quality improvement collaboratives led by the Section of Neonatology
Key Responsibilities:
Project Management Responsibilities (75%)
Manage statewide/regionwide multisite quality improvement collaboratives that include other hospital systems and non-profits.
Coordinate various sub-projects that are taking place within the broader collaborative efforts.
Conduct rigorous stakeholder and communication management tasks to recruit and maintain engagement of numerous project partners at various sites.
Coordinate submission process for Date Use Agreements (DUA) and Business Associate Agreements (BAA) to ensure regulatory compliance among all sites.
Plan, facilitate, and document steering and advisory committee meetings for the quality improvement collaboratives.
Identify, track, mitigate, and resolve all project-related issues.
Develop program/project goals and communicate goals and outcomes with a variety of stakeholders.
Participate in tactical and strategic program/project development and planning.
Research Responsibilities (25%)
Complete the consent process and enrollment of study participants.
Administer study surveys in-person, by phone, or electronically.
Conduct interviews in-person, by phone, or via Zoom.
Manage IRB application development and submission.
Complete required study documentation and reporting.
Plan, facilitate, and document research team meetings.
Work Location:
Onsite – this role is expected to work onsite and is located in Aurora, CO.
Why Join Us:
With an abundance of sunshine and mountains nearby, the Colorado Front Range is th
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