Global Clinical Project Manager Rotterdam

Resourcing Life Science

Rotterdam

On-site

EUR 70,000 - 90,000

Full time

14 days+

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Job summary

Resourcing Life Science is seeking a Global Clinical Project Manager for our Rotterdam, Netherlands location. You will lead cross-functional project teams globally and ensure adherence to Good Clinical Practices and investigator integrity throughout the study lifecycle.

The role requires 2+ years as a Clinical Project Manager in a CRO, with experience in phase II-III trials and commercial studies, and fluency in English and Dutch. Strong communication and stakeholder management are essential.

Qualifications

  • Bachelor degree in life-science.
  • Min 2 years experience as Clinical Project Manager within a CRO.
  • Experience in clinical studies phase II-III.
  • Experience in commercial studies.

Responsibilities

  • Leading cross-functional project teams globally.
  • Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
  • Monitor study timelines, patient recruitment, budget.
  • Participate in bid defence, client, investigator and team meetings.

Skills

Fluent English
Fluent Dutch
Excellent communication skills
Cross-functional leadership

Education

Bachelor degree in life-science

Job description

Company Description

Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Global Clinical Project Manager in Rotterdam.

Job Overview
  • Leading cross-functional project teams globally
  • Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures.
  • Monitor study timelines, patient recruitment, budget
  • Participate in bid defence, client, investigator and team meetings
Key Requirements
  • Bachelor degree in life-science
  • Min 2 years experience as Clinical Project Manager within a CRO
  • Experience in commercial studies
  • Experience in clinical studies phase II-III
  • Fluent English & Dutch
  • Excellent communication skills
  • FTE: 1.0

Tagged as: CPM jobs

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