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Project Manager- Decentralized Clinical Trials

  1. Mexico, Romania, Prague, Budapest, Dublin, Warsaw, Lisbon, Madrid, Slovakia
JR100685
  1. Clinical Project Management
  2. ICON Full Service & Corporate Support
  3. Hybrid: Office/Remote

About the role

This vacancy has now expired. Please click here to view live vacancies.

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.

ICON are currently seeking an experienced clinical research professional to join us as a Project Manager in our Sites and Patients Recruitment Solutions business unit. The Project Manager will collaborate with internal and external stakeholders to define, design, build and deploy innovative digital health solutions in order to support decentralized clinical trials. This is a unique opportunity to join an industry leader at the vanguard of clinical research.  

Primary Responsibilities

  • Facilitate cross functional teams to collate requirements and support the technical team in understanding the business needs.

  • Acts as a facilitator and connector between operational and technical stakeholders to achieve successful requirements definition, technology design and operational deployment

  • Leads discussion and presentation with internal and external stakeholders to gather feedback on solutions and provide feedback to Product Managers for consideration to product roadmap.

  • Participates in the definition and development of product value proposition relative to market needs.

  • Collaborate with project resources to support delivery as per agreed timelines.

  • Work collaboratively with other PMs within the team to define and develop an overall strategy to effectively influence the culture of the organization.

  • Escalate issues as they arise and actively seek resolution.

Qualifications

This position would be suitable for someone that has an in-depth understanding of the clinical trial process and the challenges that arise in different service areas, as well demonstrable experience leading effective cross-functional teams

If you are an innovator that is technologically adept, solution driven has the ability to anticipate issues before they arise, you should apply.

  • BS / BSc degree required, MBA or other advanced degree preferred

  • At least 5 years of experience in CRO setting

  • Ability to rapidly shift priorities, adjust for demands, and manage complex programs

  • Thorough knowledge of ICH-GCP, data privacy standards and local regulatory regulations regarding drug research and development required


Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, 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.

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