Local Clinical Project Manager Oncology – France

TN France; France; Sur place; EUR 45 000 - 75 000; Plein temps

Résumé du poste

An ambitious health company is seeking a Local Clinical Project Manager to join their dynamic team in France. This role offers the opportunity to drive innovation in clinical research while working in a collaborative environment that values personal growth. You will be responsible for managing clinical study documents, overseeing budgets, and ensuring successful patient recruitment. If you are passionate about improving healthcare and thrive in a fast-paced setting, this position is perfect for you. Join a forward-thinking organization that is committed to excellence and making a real impact in the field.

Qualifications

• Experience in clinical project management and regulatory compliance.
• Strong understanding of GCP and clinical trial processes.

Responsabilités

• Develop clinical study documents and manage study planning.
• Coordinate activities to ensure effective patient recruitment.
• Manage regulatory submissions and compliance with legislation.

Connaissances

Clinical Study Management

Budget Management

Regulatory Submissions

Patient Recruitment

Formation

Bachelor's Degree in Life Sciences

Master's Degree in Clinical Research

Description du poste

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Local Clinical Project Manager Oncology – France, france

Client: Excelya

Location:

Job Category: Other

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EU work permit required: Yes

Job Reference: f8bc47bfd668

Job Views: 3

Posted: 25.04.2025

Expiry Date: 09.06.2025

Job Description:

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’s leading mid-size CRO with the best employee experience. Our one-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 care means 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.

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

Main Responsibilities

• Development of clinical study documents
• Management of study planning and budget
• Selection and management of investigator sites and subcontractors
• Coordination of all activities to ensure patient recruitment
• Delivery of study results under optimal conditions of quality, timelines, and cost
• Regulatory submissions management and administrative follow-up in compliance with legislation, GCPs, and internal procedures
• Feasibility studies and investigator selection