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Clinical Team Manager
University of Wisconsin-MadisonPosted 10/20/2026full-timeMadison • Wisconsin • United StatesJuniorMid-Level💰 $75,000 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in managing oncology clinical research programs, ensuring compliance with regulations, and providing leadership to clinical research teams. Proficient in coordinating complex clinical trials, overseeing patient-related activities, and managing budgets while maintaining high standards of research integrity.
Highest-signal resume keywords
Clinical Research ManagementOncology ExperienceTheranostics KnowledgeClinical Research CertificationSupervisory Experience
About the role
Key responsibilities & impact- Function on the Management Team of an oncology clinical research program within the Clinical Research Central Office
- Support the Theranostics Disease-Oriented Team conducting clinical trials involving radiopharmaceutical therapies
- Provide clinical support, leadership, and supervision to the Theranostics Disease-Oriented Team
- Ensure research activity adheres to applicable international, federal, state, and institutional laws, policies, procedures, and requirements
- Oversee patient-related clinical activities of the research office
- Supervise Clinical Research Coordinators, Research Nurses, and/or Data Coordinators
- Coordinate complex clinical trials and collaborate across clinical, research, and specialized services
- Monitor program budgets and approve unit expenditures
- Exercise supervisory authority over at least 2.0 FTE employees
- Schedule logistics and secure resources for high-complexity and/or multiple clinical research trials
- Recruit, screen, and enroll trial participants
- Collect complex information and perform medical assessments under supervision from a medically licensed professional
- Serve as subject matter expert and main point of contact for clinical research participants
- Compose, assemble, and submit grant proposals and study protocols
- Assist with research trial reviews and develop operational protocols and work unit policies
- Collect, prepare, process, analyze, and submit participant data and samples
Requirements
What you’ll need- Minimum 2 years of experience in clinical research required
- Prior experience in oncology required
- Must either hold an approved clinical research certification or be eligible to obtain one as of the start date
- Individuals not already certified must obtain certification within 6 months of hire
- Acceptable certifications include CCRP (SOCRA), CCRA, CCRC, and ACRP-CP (ACRP)
- University sponsorship is not available, including transfers of sponsorship and TN visas
- Must maintain continuous eligibility to work in the United States
- Must provide proof of work authorization and eligibility to work
- Bachelor's Degree preferred
- Four years of experience in clinical research preferred
- Prior experience with theranostics preferred
- Supervisory/Management experience preferred
- Cover letter required
- Resume required
- Employment may require a criminal background check
- References may be requested from final candidates
Benefits
Comp & perks- Generous vacation, holidays, and sick leave
- Competitive insurances and savings accounts
- Retirement benefits
ATS Keywords
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Hard Skills
Clinical Trial CoordinationPatient RecruitmentData AnalysisMedical AssessmentGrant Proposal Writing
Soft Skills
LeadershipCollaborationCommunication
Certifications & Qualifications
CCRPCCRACCRCACRP-CP
Industry Keywords
Clinical ResearchRadiopharmaceutical TherapiesComplianceResearch ProtocolsOperational Protocols