5 дней назад
Manager, Start Up (Clinical Research)
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Manager, Start Up (Clinical Research): Managing study start-up teams, staffing, resources, and processes for clinical research projects across multiple countries with an accent on timelines, feasibility analysis, regulatory compliance, and operational efficiency. Focus on mentoring direct reports, forecasting utilization, harmonizing start-up processes, and coordinating stakeholders through study start-up, maintenance, and closeout.
Location: Taiwan
Company
supports biotech, medtech, and specialty pharma organizations in developing medicines, devices, and diagnostics through clinical research services.
What you will do
- Manage study start-up teams, staffing, resources, and timelines across multiple countries.
- Improve and harmonize study start-up, essential document maintenance, and closeout processes while maintaining quality.
- Manage, mentor, train, and evaluate direct reports, including performance objectives, career development, and staffing transitions.
- Analyze study metrics, feasibility data, costing, and utilization forecasts; provide regular updates to management.
- Support business development, proposal specifications, client presentations, and identification of out-of-scope work.
- Maintain staff alignment with company SOPs, industry regulations, time-entry guidelines, and operational procedures.
Requirements
- Undergraduate degree or international equivalent in clinical, science, or health-related studies, a licensed healthcare qualification, or equivalent work experience.
- At least 5 years of experience in the clinical research industry.
- At least 2 years of people management experience.
- Experience reviewing metrics and feasibility data, managing multiple deadlines, and applying project management principles.
- Working knowledge of FDA, European regulatory and EC procedures, ICH/GCP regulations, national and local health systems, and relevant cultural practices.
- Fluent written and verbal English required.
Nice to have
- Experience in a CRO, medical device, or pharmaceutical environment.
Culture & Benefits
- Opportunities for professional growth, training, and career development.
- Flexible work practices intended to support work-life balance.
- Participation in corporate initiatives and cross-functional knowledge sharing.
- Work in a global environment coordinating studies across multiple countries.
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