Project Director – Clinical Trials (Europe)

About the role

Allucent™ is seeking an experienced Project Director to lead clinical trial projects across Oncology, Neuroscience, Immunology and Infectious Diseases in Europe. The role is hybrid/remote and involves overseeing studies from planning through completion, ensuring safety, regulatory compliance and efficient delivery.

Key responsibilities

• Own overall quality and delivery of clinical trial projects and programs.
• Manage cross‑functional resources, budgets, financial forecasting, invoicing and out‑of‑scope activities.
• Review and approve proposal content and costing.
• Implement risk management throughout the project lifecycle.
• Negotiate with internal and external stakeholders to achieve project goals.
• Serve as primary client contact, ensuring satisfaction and alignment with scope.
• Lead and mentor project staff, support recruitment, and provide performance feedback.
• Travel up to 10% of the time, including possible international trips.

Required profile

• Minimum Bachelor’s degree in life sciences, healthcare or business; Master’s preferred.
• At least 7 years of experience in drug development or clinical research.
• 5+ years of hands‑on clinical project management, with CRA experience considered a plus.
• Deep knowledge of ICH‑GCP (R2), data privacy and local regulatory requirements.
• Strong financial acumen and administrative excellence.

Required skills

• ICH‑GCP (R2) compliance
• Clinical project management
• Budgeting and financial forecasting
• Regulatory compliance and data privacy
• Risk management

What we offer

• Opportunity to lead high‑impact trials for innovative therapies.
• Hybrid work environment with flexibility.
• Collaborative A‑team culture focused on growth and excellence.