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Clinical Research Manager
University of Wisconsin-MadisonClinical Research Manager directing K-12 clinical research for UW–Madison’s School Mental Health Collaborative. Supervising staff, ensuring compliance, developing grants, and managing program budgets.
Posted 8/25/2026full-timeMadison • Wisconsin • 🇺🇸 United StatesMid-LevelSenior💰 $95,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing clinical research protocols and trials within K-12 settings, ensuring compliance with regulations and promoting student success through effective program execution and staff supervision.
Highest-signal resume keywords
Clinical Research ManagementGrant Proposal DevelopmentBudget Development and MonitoringSupervisory ExperienceKnowledge of IRB Standards
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Research ProtocolsProgram EvaluationData ComplianceExpenditure MonitoringResearch Data DocumentationPolicy DevelopmentStandard Operating ProceduresHuman Subjects ResearchProgram EnhancementAudit Compilation
Soft Skills
Strong Written CommunicationStrong Verbal Communication
Industry Keywords
K-12 EducationSocial-Emotional SuccessBehavioral SuccessHIPAAFERPAInstitutional RegulationsPerformance ManagementProfessional DevelopmentStakeholder CollaborationCriminal Background Check
About the role
Key responsibilities & impact- Direct planning and implementation of clinical research protocols within K-12 settings
- Ensure high-quality execution of programs focused on student social-emotional and behavioral success
- Identify and solicit new internal and external research opportunities
- Promote center capabilities and recommend strategic program enhancements to leadership
- Develop and maintain clinical research policies, standard operating procedures, and operational guidelines
- Compile audits and document research data for compliance with institutional policies and procedures
- Compose, assemble, and submit grant proposals and research protocols
- Supervise at least 2.0 FTE clinical research staff, including hiring, performance management, and professional development
- Manage program functioning and fiscal health through budgets, expenditure monitoring, and resource optimization
- Plan staff implementation and ongoing quality review of clinical research trials or programs
- Collaborate with faculty, staff, investigators, and school/community stakeholders under Principal Investigator supervision
Requirements
What you’ll need- Demonstrated experience coordinating and managing clinical research trials or programs involving human subjects
- Experience exercising supervisory authority, including hiring, performance management, and professional development of staff
- Ability to compose, assemble, and submit grant proposals and research protocols in accordance with federal, state, and institutional regulations
- Knowledge of clinical research policies and procedures, including IRB standards and data privacy such as HIPAA or FERPA
- Experience developing and monitoring program budgets, including reviewing and approving expenditures
- Strong written and verbal communication skills
- Master's degree required
- Preferred degree in education, psychology, social services, education, school psychology, social work, or a related field
- Eligibility to work in the United States
- Successful applicants may be subject to a criminal background check
- Three professional references required
- Resume/CV and cover letter required
Benefits
Comp & perks- Generous paid time off
- Competitively priced health, dental, vision, and life insurance
- Tax-advantaged savings accounts
- Participation in the Wisconsin Retirement System (WRS) pension fund
- Limited remote work flexibility may be available