Manhattan WMOS Engineer
ShyftLabs
Support Manhattan WMOS implementations and operations as a WMS Engineer at ShyftLabs. ShyftLabs builds data products and digital solutions for Fortune 500 companies.
Deschide
University of Wisconsin-Madison este o universitate publică de cercetare din Madison, Wisconsin, și campusul principal al sistemului University of Wisconsin. Comunitatea sa academică și de cercetare cuprinde științele umaniste, științele exacte și domeniile aplicate, iar în cercetare se investesc anual peste 1 miliard de dolari. Universitatea îmbină educația de licență și studiile postuniversitare cu implicarea în comunitate, resursele campusului și activitățile sportive, având ca reper Ideea Wisconsin, axată pe serviciul public. Activitatea sa pune, de asemenea, accent pe diversitate, excelență incluzivă și implicarea în comunitatea extinsă.
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.
Descriere
- 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
Cerințe
- 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
Beneficii
- Substantial vacation, holiday, and sick leave allowances
- Competitive insurance plans and savings accounts
- Retirement benefits
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