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2 дня назад

Clinical Project Manager (Clinical Research)

Формат работы
hybrid
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 Research): Delivering and managing clinical studies by coordinating cross-functional teams, customers, vendors, and study plans with an accent on clinical trial compliance, quality, timelines, and financial performance. Focus on managing study risks, resolving operational obstacles, ensuring ICH GCP compliance, and accelerating milestones across project stakeholders.

Location: Amsterdam, Netherlands; at least 2 days per week at the sponsor's office in Haarlem. Candidates must be based in the listed location.

Company

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

What you will do

  • Deliver and manage smaller, less complex local clinical studies in line with contracts, SOPs, policies, and quality standards.
  • Develop integrated study management plans and coordinate cross-functional project teams.
  • Monitor milestones, timelines, risks, quality issues, contingencies, and corrective action plans.
  • Manage communications with customers, internal stakeholders, vendors, and business development representatives.
  • Oversee project financial performance, contractual obligations, forecasting, and opportunities to accelerate delivery.
  • Support staff development and mentor less experienced project team members.

Requirements

  • Bachelor's degree in life sciences or a related field.
  • At least 3 years of project management experience and 5 years of clinical research experience.
  • Knowledge of clinical trial conduct, ICH GCP, and applicable local regulations and guidelines.
  • Fluency in Dutch and English is required.
  • Strong problem-solving, communication, planning, prioritization, and decision-making skills.
  • Must be based in the listed location and willing to work at the sponsor's Haarlem office at least 2 days per week.

Culture & Benefits

  • Work with cross-functional and international teams across different geographies.
  • Focus on improving clinical trial delivery, operational excellence, quality, and patient outcomes.
  • Opportunity to support professional development through mentoring and staff development.

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