Senior Clinical Trial Manager - Oncology; Europe

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way.
Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands‑on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.

Join us!

As a Senior Clinical Trial Manager, you will lead the delivery of critical clinical site management activities across studies and regions, helping ensure research is conducted with quality, efficiency, and compliance at every stage. Your leadership will directly support the successful execution of clinical trials and contribute to bringing new therapies to patients.
In this role, you will partner closely with project management, sponsors, CRAs, and cross‑functional teams to drive study performance, oversee monitoring strategies, and ensure sites are supported from qualification through closeout. You'll play a pivotal role in risk management, team leadership, operational excellence, and the delivery of high-quality clinical outcomes.
You will also serve as a key point of contact for sponsors and study teams, providing strategic oversight, mentoring site management teams, and ensuring clinical operations remain aligned with study goals, timelines, and quality expectations.

This is a remote role open to candidates based in Europe. You will collaborate with global teams across multiple time zones.
Travel will be required on an as‑needed basis.

• Lead and coordinate clinical site management activities from study startup through database lock and study closeout.
• Partner with project management to develop monitoring strategies, establish site management targets, and ensure delivery against project goals.
• Provide leadership, guidance, and oversight to CRAs and site management team members across assigned studies and regions.
• Serve as the primary site management representative for sponsors, study teams, investigator meetings, audits, inspections, and key project discussions.
• Drive quality and compliance by overseeing monitoring activities, reviewing protocol deviations, ensuring adherence to Clinical Monitoring Plans, and maintaining inspection readiness.
• Monitor study metrics, recruitment performance, resource allocation, and operational trends to identify risks and implement effective solutions.
• Support patient recruitment efforts by tracking enrollment progress and guiding site‑specific recruitment strategies to maintain study targets.
• Ensure Trial Master File…