Research Program Coordinator

University of Wisconsin MadisonMadison, WI
Hybrid

About The Position

This position provides centralized ownership of study activation activities across the Department of Pediatrics clinical research portfolio, supporting investigator-initiated, industry-sponsored, and federally funded studies from study award or selection through activation and enrollment. The Research Program Coordinator develops, coordinates, and implements the operational infrastructure required to efficiently initiate new clinical research studies by standardizing processes, coordinating cross-functional activities, and ensuring study teams are prepared for successful study implementation. The Research Program Coordinator serves as the primary operational liaison among investigators, research staff, institutional offices, ancillary services, sponsors, and external collaborators to coordinate study start-up activities, facilitate institutional and sponsor requirements, and ensure alignment across operational, regulatory, financial, and clinical workflows. Responsibilities include coordinating study activation milestones; supporting IND/IDE preparation activities; developing and testing electronic case report forms (eCRFs); coordinating institutional agreements; facilitating research systems implementation; organizing protocol documentation; and supporting implementation across research systems and operational platforms. The position develops standardized workflows, procedures, training resources, and operational guidance that improve consistency, reduce study activation timelines, and promote efficient study implementation across the department. The coordinator also supports internal quality review processes to strengthen documentation quality, ensure adherence to institutional and sponsor requirements, and identify opportunities for continuous process improvement.

Requirements

  • Experience coordinating clinical research studies
  • Minimum two years of experience working in clinical research
  • Previous experience with OnCore, eBinders, Electronic Health Records (preferably EPIC), and/or REDCap

Nice To Haves

  • Minimum two years of experience coordinating and implementing research study start-up activities for pediatric research studies
  • Minimum two years of experience supporting pediatric, longitudinal, or multidisciplinary clinical research studies

Responsibilities

  • Coordinates the daily activities and contracts related to one or more research program(s)
  • Serves as a unit liaison and subject matter expert among internal and external stakeholder groups, collaborates across disciplines and functional areas, provides program information, and promotes the accomplishments and developments of scholars and research initiatives
  • Assists in the development, coordination, and facilitation of trainings and workshops for internal and external audiences to disseminate research program developments and information
  • Plans, develops, and implements processes and protocols to support research aims
  • Monitors program budget(s) and approves unit expenditures
  • Develops policies, procedures, and institutional agreements on behalf of the program

Benefits

  • generous vacation
  • holidays
  • sick leave
  • competitive insurances and savings accounts
  • retirement benefits
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