7 дней назад
Senior Manager Local Study Operations (Clinical Development)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Manager Local Study Operations (Clinical Development): Leading local study operations managers and delivering the country's clinical trial portfolio with an accent on portfolio execution, quality oversight, resource allocation, and regulatory compliance. Focus on developing high-performing teams, managing vendor performance, resolving country-level risks, and aligning local trial delivery with global R&D strategies.
Location: Diegem, Belgium
Company
Biotechnology and pharmaceutical company focused on clinical development and global research and development.
What you will do
- Lead and develop Local Study Operations Managers across the country portfolio.
- Oversee clinical study delivery from feasibility through close-out, including scope, timelines, budgets, risks, and quality.
- Manage Local Study Operations Manager and vendor performance, serving as the escalation point for local study challenges.
- Allocate resources and workloads across FSP and FTE personnel to optimize trial execution.
- Coordinate collaboration between study strategy, local study, and cross-functional country teams.
- Drive operational efficiency, digital innovation, knowledge sharing, and continuous improvement.
Requirements
- Doctorate degree and 2 years of clinical execution experience, or a Master’s degree and 6 years, Bachelor’s degree and 8 years, Associate’s degree and 10 years, or high school diploma/GED and 12 years.
- At least 2 years of direct people management or leadership experience involving teams, projects, programs, or resource allocation.
- Experience managing clinical operations and understanding local regulatory requirements for global clinical trials.
- Experience overseeing clinical research vendors such as CROs, central labs, or imaging vendors.
- Experience managing multiple teams, direct reports, clinical functions, or trials.
Nice to have
- Seven years of experience in life sciences or a medically related field.
- Four years of biopharmaceutical clinical research experience in a biotech, pharmaceutical, or CRO company.
Culture & Benefits
- Full-time employment.
- Focus on professional development, mentoring, and preparation for managing complex clinical trials.
- Collaborative environment involving global strategy, country leadership, and cross-functional stakeholders.
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