Назад
Company hidden
5 дней назад

Manager, Start Up (Clinical Research)

Формат работы
onsite
Тип работы
fulltime
Английский
c1
Страна
Taiwan
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
Для мэтча и отклика нужен Plus

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

hirify.global 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.

Будьте осторожны: если работодатель просит войти в их систему, используя iCloud/Google, прислать код/пароль, запустить код/ПО, не делайте этого - это мошенники. Обязательно жмите "Пожаловаться" или пишите в поддержку. Подробнее в гайде →