Clinical Trial Supply Manager

Clinical Trial Supply Manager

ICON

Sofia, Warsaw or Madrid

As a Clinical Supplies Project Manager at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

You will oversee project and programme management workstreams, ensuring deliverables meet quality and timeline expectations.

Key responsibilities include:

• Oversee the planning and execution of clinical supplies projects, ensuring timely delivery and compliance with regulatory requirements.
• Collaborate with cross-functional teams to design and implement effective strategies for clinical trial supply management.
• Monitor and analyze project timelines, budgets, and resource allocations to optimize efficiency and meet project goals.
• Address potential risks and challenges in clinical supplies logistics, proposing and implementing solutions to ensure smooth project execution.
• Foster strong relationships with internal and external stakeholders, facilitating effective communication and collaboration throughout the project lifecycle.

Your Profile:

You will have solid project and programme management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

• Bachelor's degree in a relevant field, such as pharmacy, life sciences, or supply chain management.
• Proven experience in clinical supplies project management within the pharmaceutical or biotech industry.
• Strong understanding of regulatory requirements related to clinical trial supply management.
• Excellent organizational and communication skills, with the ability to guide cross-functional teams and drive project success.
• Problem-solving mindset, with the ability to adapt to changing project dynamics and implement effective solutions.