2 дня назад
Sr Mgr Local Study Operations (Clinical Research)
150 773 - 203 987CAD
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Sr Mgr Local Study Operations (Clinical Research): Leading country-level clinical study portfolio delivery through Local Study Operations Managers with an accent on trial execution, risk oversight, resource allocation, and regulatory quality. Focus on developing LSOM teams, managing vendors and complex escalations, and driving continuous improvement across clinical operations.
Location: Mississauga, Canada
Salary: CAD 150,773–203,987 per year
Company
is a biotechnology company developing, manufacturing, and delivering medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.
What you will do
- Lead delivery of the country study portfolio from feasibility through study close-out.
- Oversee Local Study Operations Managers, vendors, portfolio scope, timelines, budgets, risks, and quality.
- Serve as the primary escalation point for local study challenges and drive issue resolution.
- Mentor, train, and support the professional development of LSOMs while building a high-performing team.
- Coordinate collaboration among study strategy, local study, country, and cross-functional teams.
- Lead operational efficiency, best-practice sharing, resource allocation, and continuous improvement initiatives.
Requirements
- Doctorate degree with 2 years of clinical execution experience, or a master's degree with 6 years, bachelor's degree with 8 years, associate's degree with 10 years, or high school diploma/GED with 12 years.
- At least 2 years of direct people management or leadership experience involving teams, projects, programs, or resource allocation.
- Advanced English proficiency required.
- Experience in clinical execution, clinical operations, risk and quality oversight, and regulatory compliance.
- Ability to manage resources, workloads, vendors, escalations, and complex clinical trial delivery.
Nice to have
- Seven years of experience in life sciences or a medically related field, including four years in biopharmaceutical clinical research.
- Experience managing multiple teams or direct reports across clinical functions and trials.
- Experience overseeing CROs, central laboratories, imaging vendors, or other clinical research vendors.
- Experience managing clinical operations across relevant geographies and understanding local regulatory requirements for global clinical trials.
Culture & Benefits
- Collaborative, innovative, and science-based working environment.
- Health and welfare plans for eligible staff and dependents.
- Financial plans with opportunities to save for retirement and other goals.
- Work-life balance support and career development opportunities.
- Reasonable accommodation is available during the application and interview process.
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