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Project Manager, Data Management (Remote)

North Wales,Mexico City,Canada
Reference: JR073589

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.


Due to new business wins, we are currently recruiting for a Project Manager to join the Data Management team. The successful applicant will be responsible for the management of data teams, studies and programmes of studies. This will include providing planning estimates for project scope, schedule and resource requirements ensuring programs are properly budgeted, estimated and scheduled. Working closely with other departments to ensure all data collected during trials is managed and meet regulatory guidelines

Location Options

  • United States (home-based OR office-based)
  • Mexico (office-based with some remote flexibility)
  • Canada (home-based)

Highlights of Key Responsibilities:

  • Oversee the day-to-day activities and task management of the project team to ensure that a focus on quality, budget and timelines on each project is reached and maintained
  • Lead and motivate a team according to organizational goals
  • Plan, implement and deliver the project in accordance with the contract agreed with the sponsor
  • Prepare and manage the overall project budget throughout the life cycle of the project, taking overall responsibility for cost control, timelines and project quality
  • Typically responsible for handling multiple studies running concurrently
  • Deliver Project to Quality, Timeline and Budget Requirements
  • Negotiate with clients and/or external customers/departments in relations to timelines and key deliverables
  • Research and recommend new data management processes, which address customer needs and key business objectives


  • 6+ years of clinical data management experience
  • 3+ years as a lead or point of contact for day to day activity on studies regarding set-up and close-out tasks
  • Experience with at least one CDMS (ex: Rave, Inform, OCRDC)
  • Proven leadership skills
  • Knowledge of FDA regulations
  • Experience working with tight deadlines

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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