Senior Research Program Manager

Posting Information

• Department:
  Sch of Nursing-440100
• Career Area:
  Research Professionals
• Posting Open Date: 02/26/2026
• Final date to receive applications: 03/12/2026
• Open Until Filled:
  No
• Position Type:
  Permanent Staff (EHRA NF)
• Working Title:
  
  Senior Research Program Manager
• Appointment Type: EHRA Non-Faculty
• Position Number:
• Vacancy
• Full Time/Part Time:
  Full-Time Permanent
• FTE: 1
• Hours per week: 40
• Position Location:
  
  North Carolina, US
• Hiring Range:
  Dependent on Qualifications
• Proposed
  
  Start Date:
  
  03/23/2026

A global higher education leader in innovative teaching, research and public service, the University of North Carolina at Chapel Hill consistently ranks as one of the nation's top public universities
. Known for its beautiful campus, world-class medical care, commitment to the arts and top athletic programs, Carolina is an ideal place to teach, work and learn.

One of the best college towns and best places to live in the United States, Chapel Hill has diverse social, cultural, recreation and professional opportunities that span the campus and community.

University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks for numerous retail, restaurant and performing arts discounts, savings on local child care centers and special rates on select campus events. UNC-Chapel Hill offers full-time employees a comprehensive benefits package
, paid leave, and a variety of health, life and retirement plans and additional programs that support a healthy work/life balance.

This position requires advanced professional knowledge in global or public health, nursing, health sciences, or health informatics, applying theoretical frameworks and scientific methodologies to manage complex health services, digital health, and implementation-science research programs. The Research Associate independently operationalizes research protocols; integrates human subjects protections, clinical workflow principles, and research compliance requirements; and ensures methodological rigor across quantitative, qualitative, and digital-health data streams.

The role requires specialized academic training to translate scientific aims into operational workflows, manage multi-site study infrastructure, analyze research data, and develop scholarly products such as manuscripts, abstracts, and sponsor-required reports.

The position involves duties that are inherently specialized, including research protocol development, IRB regulatory oversight, data governance, digital health implementation, multimodal data management, and contributions to peer reviewed dissemination.

Relevant post-Baccalaureate degree required (or foreign degree equivalent); for candidates demonstrating comparable independent research productivity or professional-level background in sponsored research administration, will accept a relevant Bachelor's degree (or foreign degree equivalent) and 3 or more years of relevant experience in substitution.

• Master's degree in Global Public Health, Public Health, Health Informatics, Nursing, Epidemiology, or another health related scientific discipline.
• Demonstrated experience coordinating research projects, including protocol implementation, timelines, and multi-stakeholder communication.
• Working knowledge of human subjects research requirements and research compliance (IRB submissions, informed consent processes, HIPAA and PHI handling, and required trainings).
• Experience with research data workflows, including data collection tools (for example, REDCap or equivalent), data quality checks, and generation of routine study reports.
• Strong written and verbal communication skills, including ability to draft study documentation and summarize findings for scientific and operational audiences.
• Ability to manage multiple priorities, work independently, and collaborate effectively in a team-based research environment.

• Experience supporting federally funded research (NIH, AHRQ, CDC, HRSA) and multi-site study operations.
• Experience with digital health, virtual care, clinical workflow evaluation, implementation science, or quality improvement research.
• Experience with EHR data requests, data governance processes, and/or analytic platforms; familiarity with basic quantitative and qualitative methods.
• Demonstrated experience drafting IRB materials, SOPs, data dictionaries, and contributing to abstracts, manuscripts, and grant applications.
• Proficiency with common research productivity tools (Microsoft Office, SharePoint/Teams), and project management tools (for example Smartsheet, Asana, Trello).

Work is primarily performed in an office or remote office environment with prolonged periods of sitting and computer use. Must be able to communicate effectively…