ICON Clinical Research

Clinical Trial Manager- RWE Late Phase EU wide

23 Jul 2021
30 Jul 2021
Full Time
Contract Type
Experience Level
Experienced (non-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.

At ICON, we are looking for specialist experience in Late Phase clinical studies to run Clinical Trial Management.

As a Clinical Trial Manager at ICON, you will lead clinical deliverables, oversee a global clinical team within Phase IIIb-IV projects. Act as the point of contact for the internal team and client, develop the clinical plan, implement protocol training requirements and maintain key clients relationships.

Your responsibilities will include:
  • Lead the global team clinical team (including CRA's) on projects, providing the team with direction guidance
  • Build necessary project training for assigned clinical staff and track relevant clinical project deliverables, use appropriate tracking and budgeting tools
  • Update the sponsor clinical team with key aspects of the project actions and updates

What you need
  • ICON is seeking experience in delivering late phase clinical studies as a CTM
  • University/Bachelor's Degree in medicine, science or equivalent degree/experience
  • Thorough understanding of ICH GCP and relevant regulations for the conduct of clinical trials
  • Experience in Study Start Up preferred
  • Due to the nature of this position, the employee will travel approx. 25%. Therefore, dependent on the employee's location, the employee may be required to possess a valid Driver's license

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.