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University of Wisconsin-Madison

Clinical Team Manager

University of Wisconsin-Madison

. Serve as a subject matter expert and main point of contact for clinical research participants .

Posted 10/19/2026full-timeMadison • Wisconsin • United StatesJuniorMid-Level💰 $75,000 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in clinical research management, including participant recruitment, data collection, and adherence to research protocols. Proven ability to supervise teams, manage budgets, and improve operational processes within clinical trials.

Highest-signal resume keywords
Clinical Research CertificationParticipant RecruitmentBudget ManagementSupervisory ExperienceOncology Experience

ATS Keywords

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Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard Skills
Clinical Research ProceduresData AnalysisMedical AssessmentsOperational Protocol DevelopmentPerformance Management
Soft Skills
CommunicationLeadershipProblem-Solving
Certifications & Qualifications
CCRPCCRACCRCACRP-CP
Industry Keywords
Clinical TrialsParticipant EnrollmentResearch ProtocolsBudget MonitoringOncology

About the role

Key responsibilities & impact
  • Serve as a subject matter expert and main point of contact for clinical research participants
  • Provide information regarding research procedures, expectations, and inquiries
  • Schedule logistics and secure resources for high-complexity or multiple clinical research trials
  • Supervise at least 2.0 FTE employees, including hiring, performance management, assigning work, and approving hours
  • Monitor program budgets and approve unit expenditures
  • Recruit, screen, and enroll trial participants
  • Collect complex information, perform medical assessments, and answer detailed questions under supervision from a medically licensed professional
  • Collect, prepare, process, analyze, and submit participant data and samples while adhering to research protocols
  • Assist with review of current research trials and development of operational protocols and work unit policies
  • Recommend improvements to leadership

Requirements

What you’ll need
  • Minimum 2 years of experience in clinical research 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 successfully 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 without employer sponsorship
  • Must provide proof of work authorization and eligibility to work
  • Employment may require a criminal background check
  • Bachelor’s degree preferred
  • Four years of experience in clinical research preferred
  • Prior experience in oncology strongly preferred
  • Supervisory/Management experience preferred

Benefits

Comp & perks
  • Generous vacation, holidays, and sick leave
  • Competitive insurances and savings accounts
  • Retirement benefits
  • Opportunities for skill development and advancement
  • Supportive, collaborative environment