University of Wisconsin-Madison
University of Wisconsin-Madison
University of Wisconsin-Madison ir publiska pētniecības universitāte Medisonā, Viskonsinas štatā, un Viskonsinas Universitātes sistēmas vadošā pilsētiņa. Tās akadēmiskā un pētniecības kopiena aptver humanitārās zinātnes, dabaszinātnes un lietišķās disciplīnas, un pētniecībā ik gadu tiek ieguldīts vairāk nekā 1 miljards ASV dolāru. Universitāte apvieno bakalaura un maģistra studijas ar darbu kopienas labā, universitātes pilsētiņas resursiem un sportu, vadoties pēc Viskonsinas idejas, kas uzsver sabiedrisko kalpošanu. Tās darbā svarīga ir arī daudzveidība, iekļaujoša izcilība un iesaiste plašākā kopienā.

Clinical Research Manager – Madison, Wisconsin (Hybrid)

Lead compliant clinical trials and research operations for the University of Wisconsin–Madison’s reproductive health programs. Oversee staff, budgets, protocols, grants, regulatory requirements, and collaborations across clinical research initiatives.

Apraksts

  • Coordinate staff delivery of protocols and continuing quality reviews for basic and moderately complex clinical research trials or programs
  • Create and track program budgets while reviewing and authorizing expenditures
  • Manage at least 2.0 full-time equivalent employees, including recruitment, performance oversight, disciplinary actions, and time approvals
  • Prepare and submit grant applications and research protocols in line with applicable regulations
  • Organize audits and maintain research documentation to support compliance with institutional policies and procedures
  • Evaluate research portfolios and accounts, identify internal and external funding opportunities, highlight unit capabilities, and advise leadership on strategic improvements
  • Direct the strategic planning and day-to-day operations of clinical research programs
  • Manage clinical trial execution and regulatory compliance
  • Work with investigators, sponsors, regulators, and institutional partners

Prasības

  • At least five years of clinical research or clinical trial management experience by the start date
  • Working knowledge of HIPAA, FERPA, GCP, ICH/FDA compliance, IRB procedures, and the clinical trial lifecycle
  • Ability to manage schedules, budgets, risks, and several concurrent studies
  • Experience leading cross-functional teams, addressing deviations and issues, and working with sponsors, sites, and stakeholders
  • Proficiency with EDC, Florence, OnCore, Team Work, REDCap, Arrow, RAMP, Qualtrics, Excel, and Advarra Participant Payments
  • Highly organized, quality-focused, detail-oriented, adaptable, and capable of ethical, sound decision-making
  • Master’s degree preferred, ideally in life science or healthcare
  • Resume and cover letter required
  • Successful completion of an initial caregiver check and renewal every four years under Wisconsin Caregiver Law
  • Ongoing authorization to work in the United States is required; university sponsorship is unavailable
  • Professional references will be requested from finalists

Priekšrocības

  • Substantial vacation, holiday, and sick leave allowances
  • Competitive insurance plans and savings accounts
  • Retirement benefits

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