Senior Clinical Supplies Project Manager

 Posted an hour ago
  
 Poland
  
⭐ 5-10 years experience
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AI Summary

Lead the planning and execution of clinical supplies projects, managing timelines, budgets, and resource allocation. Coordinate with cross-functional teams and suppliers to ensure the timely delivery of materials for clinical trials.
E2E Supply Planner

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Senior Clinical Supplies Project Manager at ICON, you will lead and manage clinical supplies projects to ensure timely and efficient delivery of materials for clinical trials.

What You Will Do:

Your focus will be on coordinating project and programme management delivery, resolving issues, and developing team capability.

Key responsibilities include:

  • Leading the planning, execution, and management of clinical supplies projects, including timelines, budgets, and resource allocation.
  • Collaborating with cross-functional teams to develop supply strategies that align with study requirements and regulatory guidelines.
  • Overseeing supplier relationships, negotiating contracts, and ensuring high-quality and timely delivery of clinical supplies.
  • Monitoring project progress and performance metrics, identifying risks, and implementing mitigation strategies as necessary.
  • Providing leadership and guidance on best practices in clinical supply management and project execution.

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 supply chain management, logistics, life sciences, or a related discipline
  • Extensive experience in clinical supplies management or project management, preferably within the pharmaceutical or biotechnology industry.
  • Strong understanding of clinical trial processes and regulatory requirements related to clinical supplies.
  • Excellent organizational and problem-solving skills, with the ability to manage multiple projects simultaneously.
  • Strong communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.

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.

Are you a current ICON Employee? Please click here to apply

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