Clinical Supplies PM
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 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 program 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 program 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:
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
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.
We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
