ICON Clinical Research

Clinical Supplies Manager

22 Feb 2021
12 Mar 2021
Full Time
Contract Type
Experience Level
Experienced (non-manager)
Clinical Supplies Manager - can be homebased in EU or the US

At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.

Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.

The role
  • Oversee supply and pharmaceutical development activities, with respect to technical, quality, timing and cost standpoint on behalf of the client
  • Interact closely with other ICON divisions and clients as part of the project team
  • Provide guidance to IMP management, supply strategies, supply demand planning and forecast, dosing, dispensing and formulation considerations
  • Advise, prepare and review study specific procedures, IP Management Plans and Dosing Instructions and agreement for all aspects of IP supply activities
  • Generate IP manuals, to support use of the IMP at clinical sites
  • Ensure necessary training in the receipt, storage, handling and preparation of IMP, as appropriate

What you need:
  • Bachelor's degree, licensed Pharmacist desirable
  • Clinical supply management experience, including knowledge of GMP/GDP/GCP, global regulatory requirements relating to pharmaceutical and clinical supplies
  • Able to demonstrate experience in the evaluation and procurement of marketed drug product
  • Previous experience in manufacturing operations, batch record review and approval
  • Client facing experience, ensuring our delivery meets the project expectations and coordinating regular meetings to update the client on the project status

Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.