As a Project Manager you will have the opportunity to work with one of the world’ s leading pharma & biotech companies, helping them advance new drugs and devices.

You will play a vital client facing line management role, embedded in our clients business. You will be responsible for the management of day to day biostatistics activities, ensuring everyone is well-trained on ICON standard processes, and promoting efficiency, quality, and timeliness in project work.

You will be joining one of the global healthcare leaders that has been discovering and developing medicines and treatments for well over a century. You will be part of a global team that is committed to make life better for people around the world. We share a vision of bringing treatment and medicine to millions alongside develop healthcare knowledge and improve live.

What you will be doing:

The Project Manager has responsibility for one or more studies of moderate complexity generally with responsibility for all study management aspects of assigned studies.

• Leads and manages the tactical execution of one or more clinical studies from study startup through database release.
• Provides quality oversight to the Contract Research Organization (CRO) and of the CRO deliverables related to study execution.
• Leads and coordinates the execution of a clinical trial from Study start-up through Database release and inspection readiness to ensure timely delivery of quality study data.
• Provide leadership to the teams in the setting of realistic recruitment targets and delivery milestones as the single point of accountability for detailed study start-up and monitoring plans and for delivery to the agreed plans.
• Works with functional lines and directly with CRO line functions to resolve or triage site level issues. The Study Manager will drive decision making and work closely with the Clinical Study Team Lead to provide input to operational strategy.

• The Senior Project Manager is a core member of the Study Team and will represent the CRO on matters of study execution.

You are:

• • Bachelor's degree in the health field.
  • Experience as Project Manager for global clinical studies managing budget and vendors in CROs or pharma companies.
  • Fluent English level.

What ICON can offer you:

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits

At ICON, diversity, inclusion & belonging are fundamental to our culture and values. Our rich diversity makes us more innovative which helps us better serve our people, patients, customers, and our communities. We're proud of our diverse workforce and the work we’ve done to become a more inclusive organisation. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON 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.

https://careers.iconplc.com/reasonable-accommodations

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless - there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.