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Excelya recrutement

Senior Clinical Project Manager H/F Excelya

  • Paris - 75
  • CDI
  • Bac +5
  • Industrie Pharmaceutique • Biotechn. • Chimie
  • Exp. 3 ans min.
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Les missions du poste

Senior Clinical Project Manager

At Excelya, we are seeking an experienced Senior Clinical Project Manager to lead and oversee complex clinical trials from initiation to close-out, ensuring adherence to timelines, budgets, and quality standards. This role offers the opportunity to work within a vibrant team focused on delivering impactful clinical research in a collaborative and innovative environment.

Key Responsibilities:

    • Lead and coordinate oncology clinical studies from setup to closeout
    • Contribute to protocol and clinical document writing
    • Manage timelines, budgets, regulatory submissions, and study deliverables
    • Coordinate internal and external stakeholders (sites, CRAs, partners)
    • Ensure patient safety, data quality, and regulatory compliance
    • Organize project meetings, reporting, and performance tracking
    • Supervise and support project teams (CRAs, study coordinators)

Le profil recherché

Why Join Us?

At Excelya, we combine passion for science with enthusiasm for teamwork to redefine excellence in healthcare.

Here's what makes us unique-

We are a young, ambitious health company representing 900 Excelyates, driven to become Europe'sleading mid-size CROwith thebest employee experience. Ourone-stop provider service model-offering full-service, functional service provider, and consulting-enables you to evolve through diverse projects. Working alongside preeminent experts, you will help improve scientific, operational, and human knowledge to enhance the patient's journey.

Excelling with caremeans benefiting from an environment that values your natural talents, pushes boundaries with audacity, and nurtures your potential, allowing you to contribute fully to our shared mission.

Requirements:

  • Extensive and strong experience in clinical project management within pharma or CRO
  • Strong leadership, communication, and organizational skills.
  • Proven track record in managing clinical trials on time and within budget.
  • In-depth knowledge of ICH-GCP guidelines and regulatory environment.
  • Ability to work effectively with cross-functional teams and manage multiple priorities.
  • Degree in Pharmacy, Life Sciences, or related field.
  • Fluency in English

Bienvenue chez Excelya

Excelya is an independent partner that serves Biotech, Pharma, and Medical Device organizations with a comprehensive range of full-service CRO, FSP, and Resourcing solutions guided by our values Energy, Care and Audacity.

Founded in 2014 and headquartered in Paris, France, Excelya has a global team of 900+ experts who understand the critical needs of clients to provide bespoke and robust trial solutions across a broad spectrum of therapeutic areas.

We take a one-team approach to work: our shared success is the result of collaboration at every stage of a project, from regulatory affairs and clinical operations to quality assurance and strategic development.

Excelya is committed to helping our clients deliver life-changing therapies collaboratively, so we can transform tomorrow together.

Publiée le 27/04/2026 - Réf : 10e1b782-514f-4e33-86c7-fd3d14eac1e4

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