Clinical Supplies Project Manager

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.
 

Clinical Supplies Project Manager

We are looking for a Clinical Supplies Project Manager to provides scientific, technical and regulatory support to projects that have significant Pharmaceutical Supply Management, Chemistry, Manufacturing and Control (CMC) activities associated with them and to act as the lead on appropriate project teams. You will be managing global pharmaceutical supply for all phases and pharmaceutical development activities on-going at contract facilities with respect to technical, quality, timing and cost standpoint on behalf of our clients.

• Oversee labelling, packaging and distribution activities of CMO including review and approval of labelling / packaging records and distribution plans.
• Oversee recall, returns and destruction activities, as appropriate
• Oversee the procurement of marketed drug product, such as comparators performed by an approved vendor and ensuring together with GRA / SSU that all study specific regulatory requirements are met.
• Perform Batch Record Review and Approval, as applicable.
• Manage temperature deviation, product complaints and recalls, as delegated by the client.
• Gap analysis of processes relating to pharmaceutical supplies for applicable project teams.
• Participates in the discussions of objectives and scope of prospective projects with potential clients.
• Maintain confidentiality of management information as appropriate.
• Liaise with other managers to improve the effectiveness of the organisation
• Travel (approximately 10%) domestic and/or international.
• To undertake other reasonably related duties as may be assigned from time to time.

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.