Global Clinical Project Manager

Excelya

Global Clinical Project Manager overseeing international Phase I–III trials for Excelya. Responsible for timelines, budgets, compliance, and collaboration with global study teams.

Posted 7/17/2026full-timeParis • 🇫🇷 FranceMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading global clinical trials, managing CROs, and ensuring compliance with ICH-GCP standards. Proficient in project management, risk mitigation, and stakeholder collaboration to drive successful study execution.

Highest-signal resume keywords

Global Clinical Trial ManagementICH-GCP ComplianceCRO ManagementProject ManagementClinical Operations

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial RegulationsStudy Plan DevelopmentRisk ManagementProtocol DevelopmentBudget ManagementStudy ExecutionVendor SelectionTrial Master File OversightPhase I–III Clinical TrialsQuality Standards

Soft Skills

LeadershipStakeholder ManagementCollaborationCommunicationProblem-Solving

Industry Keywords

Life SciencesClinical TrialsRFP ProcessesAudit SupportInspection Readiness

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Lead and coordinate global study teams to ensure the successful delivery of clinical trials.
Develop and manage study plans, timelines, budgets, resources, risks, and mitigation strategies.
Select, manage, and oversee CROs and third-party vendors, including participation in RFP processes and vendor selection.
Drive study execution from protocol development through study close-out and archiving.
Identify risks, implement corrective actions, and ensure compliance with quality standards and ICH-GCP requirements.
Review and contribute to key clinical study documents.
Facilitate study team meetings and ensure follow-up of actions and decisions.
Collaborate with cross-functional stakeholders to ensure efficient study conduct and patient recruitment strategies.
Ensure inspection readiness and support audits and regulatory inspections.
Maintain oversight of Trial Master File (TMF) completeness and study documentation quality.

Requirements

What you’ll need

Degree in Life Sciences or a related discipline.
Very strong experience in Clinical Operations and as a Global Clinical Trial Manager or equivalent role.
Proven experience leading international Phase I–III clinical trials.
Strong experience managing CROs and external vendors.
Solid knowledge of ICH-GCP, clinical trial regulations, and quality standards.
Experience with RFP processes and vendor selection.
Excellent project management, leadership, and stakeholder management skills.
Ability to work effectively in a matrix organization.

Benefits

Comp & perks

Why join us?
At Excelya, we combine a passion for science with the enthusiasm of teamwork to redefine excellence in healthcare.
Here's what makes us unique:
We are a young and ambitious healthcare company, bringing together 900 Excelyates, driven by the goal of becoming the leading mid-sized CRO in Europe, while offering the best employee experience.
Our "one-stop provider" service model—combining full-service, functional service provider, and consulting—allows you to grow through diverse and stimulating projects. By collaborating with leading experts, you will contribute to the development of scientific, operational, and human knowledge, all in service of improving the patient journey.
Excelling with kindness means evolving in an environment that values your natural talents, encourages boldness, pushes boundaries, and cultivates your potential, so that you can fully contribute to our shared mission.