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Senior Manager, Clinical Trial Management

  1. Sofia, Prague, Budapest, Dublin, Riga, Warsaw, Lisbon, Bucharest, Belgrade, Barcelona, Madrid, Reading
JR100066
  1. ICON Full Service & Corporate Support
  2. Clinical Operations Management
  3. Remote

About the role

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Senior Manager, Clinical Trial Management MEDICAL DEVICES

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:

Provide direction and accountability for the operational teams and their delivery at regional and site level.

• Resourcing, line management, training, functional delivery and input on discussions around quality and operational delivery measurements within the Clinical Operations group

• Conduct regular discussions with CTM  direct reports and lead team meetings at regional and manager team level.

• Assist with training for CTM Managers and Associates as required.

• Contact for region in regard to operational questions and escalations.

• Work with Director/Senior Director and/or VP Clinical Operations to communicate all critical issues, business growth opportunities, developing key relationships as well as providing input regarding budgeting discussions to drive productivity and quality within the region.

• Represent Clinical Operations at Sponsor and internal audits.

You will need:
• 4 year degree or equivalent combination of education & experience
Experience driving the clinical deliverables of a study for medical devices and/or IVD

Prior Line management experience of CRAs or CTMs

• Subject matter expertise in the designated therapeutic area
• Prior monitoring experience is preferred
• Ability to travel up to 20%
• Fluent in English - both written & verbal


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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