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Barrington James

Senior Clinical Project Manager

Barrington James
Luxembourg · Contract · Mid-Senior

We're Hiring!


Job Title: Freelance Senior Clinical Project Manager – Benelux Region

Location: Remote/Hybrid (BENELUX based preferred)

Contract Type: Freelance

Reporting To: Director of Clinical Operations / Clinical Program Lead



Position Overview:

We are seeking a Freelance Senior Clinical Project Manager with proven experience leading multi-country clinical trials across the Benelux region. This role is ideal for a seasoned professional who thrives in a flexible, autonomous environment and can immediately contribute to ongoing or upcoming studies. The Sr. CPM will be responsible for overseeing all aspects of clinical trial delivery, including project planning, execution, team coordination, vendor oversight, and regulatory compliance.


Key Responsibilities:

  • Independently manage end-to-end clinical trial activities across multiple Benelux countries.
  • Act as the primary project contact for both internal teams and external stakeholders (CROs, vendors, investigators).
  • Oversee regulatory submissions, site activations, enrolment tracking, and clinical monitoring.
  • Ensure studies are conducted in accordance with ICH-GCP, local regulations, and sponsor SOPs.
  • Monitor project timelines, scope, and budget; escalate risks and implement mitigation strategies.
  • Manage CRO and vendor performance through regular meetings, KPIs, and deliverables tracking.
  • Lead study team meetings and provide regular progress reports to sponsor leadership.
  • Support audits, inspections, and quality reviews as needed.

Requirements:

  • Bachelor’s or Master’s degree in Life Sciences or related discipline.
  • 8+ years of experience in clinical project management, with a strong focus on Benelux trials.
  • Prior freelance or consulting experience preferred.
  • Proven ability to manage complex, multi-country Phase I–IV studies.
  • Solid understanding of clinical development processes, ICH-GCP, and regional regulatory environments.
  • Strong organizational and communication skills, with the ability to manage multiple priorities.
  • Fluent in English, (additional European languages are a plus).
  • Comfortable working remotely with cross-functional global teams.
  • Availability to travel within Benelux (up to 20%), if required.
  • Must have appropriate business registration, insurances and ability to invoice


Please attach CV to apply

Key Skills

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Posted
Jul 28, 2025
Type
Contract
Level
Mid-Senior
Location
Luxembourg

Industries

Pharmaceutical Manufacturing Biotechnology Research

Categories

Management

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