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 global clinical research programs with an accent on timelines, feasibility analysis, regulatory compliance, and operational efficiency. Focus on coordinating multiple countries, mentoring direct reports, forecasting utilization, harmonizing start-up processes, and communicating with clients and stakeholders.
Location: South Korea
Company
supports biotech, medtech, and specialty pharma organizations in developing medicines, medical devices, and diagnostics through clinical research services.
What you will do
- Manage study start-up teams, staffing, resources, utilization forecasts, and project timelines across multiple countries.
- Improve and harmonize processes for study start-up, essential document maintenance, transition planning, and closeout while maintaining quality.
- Manage, mentor, train, and evaluate direct reports, including performance objectives, career development, and time-entry guidance.
- Analyze metrics, feasibility data, costing, and out-of-scope activities to support planning, productivity, and cost control.
- Contribute to business development, proposal specifications, client presentations, and cross-functional corporate initiatives.
- Maintain compliance with company SOPs, industry regulations, and study start-up procedures while preparing reports and presentations.
Requirements
- Undergraduate degree or equivalent work experience in clinical, science, or health-related fields; licensed healthcare professionals are also considered.
- At least 5 years of clinical research industry experience.
- At least 2 years of people management experience.
- Experience with analytical review of metrics and feasibility data, project management principles, and web-based communication tools.
- Working knowledge of ICH/GCP regulations, FDA and European regulatory procedures, and relevant national or local healthcare systems.
- Fluent verbal and written English required.
Nice to have
- CRO, medical device, or pharmaceutical experience.
Culture & Benefits
- Opportunities for professional growth, training, and career development.
- Flexible working practices designed to support work-life balance.
- Ability to influence working methods and contribute ideas to company initiatives.
- Global collaboration across clinical research teams and countries.
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