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ICON

ior Clinical Supplies Project Manager

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Found by HiredNow AI on 24 Sept 2026. Subscribers saw it first.

About the role

Senior Clinical Supplies Project Manager Home based UK

  • At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
  • As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.
  • 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.
  • Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

  • ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
  • Benefits may include: Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable

Retirement and pension plans

  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways
  • Benefits may vary depending on role and location.
  • Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

  • ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
  • If you require reasonable accommodations during the recruitment process, please let us know or submit a request here
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  • Are you a current ICON Employee? Please click here to apply
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