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5 дней назад

Clinical Project Manager (Clinical Trials)

Формат работы
onsite
Тип работы
fulltime
Грейд
middle
Английский
b2
Страна
Netherlands
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Clinical Project Manager (Clinical Trials): Delivering multi-country clinical studies for new drugs and medical devices with an accent on regulatory compliance, recruitment, quality, timelines, and financial performance. Focus on leading cross-functional teams, managing customer and vendor relationships, controlling project risks and scope, and solving operational challenges across clinical trial delivery.

Location: Amsterdam, Netherlands

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Lead the delivery of multi-country and multi-regional clinical studies in accordance with contracts, protocols, SOPs, ICH-GCP, and applicable regulations.
  • Develop study management plans, set objectives, coordinate cross-functional teams, and support milestone achievement.
  • Manage recruitment strategies, project risks, contingencies, quality issues, corrective actions, and change control.
  • Act as the primary contact for customers and vendors, lead project communications, and present project information to internal and external stakeholders.
  • Manage clinical project finances, including estimates at completion, scope changes, forecasts, and opportunities to accelerate revenue.
  • Build and develop clinical teams, plan resources, mentor less experienced project members, and contribute to performance feedback.

Requirements

  • At least 3 years of relevant experience managing multi-country clinical trials in a CRO or pharmaceutical company, or equivalent functional or people-management experience.
  • Bachelor’s degree in life sciences.
  • Advanced knowledge of clinical trial conduct, including ICH-GCP, EU CTR, EMA regulations, broad protocol knowledge, and clinical research requirements.
  • Good command of English and Dutch is required.
  • Strong leadership, presentation, communication, organization, prioritization, collaboration, and customer service skills.
  • Experience with project financials and strong proficiency in Microsoft Office applications, including Word, Excel, and PowerPoint.

Culture & Benefits

  • Work with cross-functional and international clinical teams across multiple geographies.
  • Contribute to the development and commercialization of medical treatments and improved patient outcomes.
  • Support professional development through mentoring and participation in learning and development activities.
  • Operate in an environment focused on client service, collaboration, communication, innovation, and ownership.

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