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(Senior) Clinical Trial Manager - CNS/Rare Diseases

  1. Sofia, Dublin, Lisbon, Bucharest, Barcelona, Madrid, Reading
JR120746
  1. ICON Full Service & Corporate Support
  2. Clinical Trial Management
  3. Hybrid: Office/Remote

About the role

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.
 

Job Title: Clinical Trial Manager - CNS and Rare Diseases

Company: ICON

Locations can be considered:

Georgia, Poland, Bulgaria, South Africa, Ireland, Spain, UK, Romania, Latvia, Lithuania, Hungary, Serbia, Portugal, Slovakia

Responsibilities:

  • Lead clinical aspects of designated projects, ensuring adherence to budget and timelines.
  • Primary point of contact for the clinical aspects of designated projects and responsible for developing successful cross-functional relationships with internal and external stakeholder
  • Drive process improvement initiatives to enhance efficiency and value.
  • Oversee clinical metrics and ensure quality standards are met.
  • Manage clinical project team to optimize performance and productivity.
  • Participate in clinical risk planning and resolution.
  • Maintain Trial Master File and ensure compliance with SOPs.
  • Participate in hiring and business development activities.
  • Travel domestically and internationally as required (approximately 25%).

Qualifications:

  • Bachelor's degree in a related field (advanced degree preferred).
  • years of experience in clinical project management.
  • Strong communication and leadership skills.
  • Ability to manage multiple priorities in a fast-paced environment.
  • Knowledge of clinical trial processes and regulations.



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.

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