Senior Clinical Project Manager leading oncology clinical studies from set-up to close-out at Excelya. Ensuring timelines, budgets, and quality standards in a collaborative team environment.
Responsibilities
**Key Responsibilities:**
Lead and coordinate oncology clinical studies from set‑up to close‑out
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)
Requirements
**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
Benefits
**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.
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