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Proj Manager, Data Management

Madrid, Spain, Poland, Warsaw, Homeworking
Start date
12 Aug 2022
Closing date
25 Aug 2022

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Clinical Research, Clinical Development
Full Time
Contract Type
Experience Level
Experienced (non-manager)
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Job Details

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.

Project Manager, Data Management

*Remote working or office based - Spain, Poland, Portugal or UK*

This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.

Overview of Role

To manage the activities of data management studies and staff in a manner that ensures all timeframes and targets are met to the sponsor's satisfaction and that costs are kept under control.

  • Manage and Develop Team Capability
  • 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 organizationalgoals.
  • Manage and appraise all staff under jurisdiction.
  • Deliver Project to Quality, Timeline and Budget Requirements
  • Plan, implement and deliver the project in accordance with the contract agreed with the sponsor.
  • Manage projects in a timely manner in adherence with ICON SOPs, SSPs and appropriate regulations and liaise with other departments and project managers as necessary to achieve this.
  • Determine the best method to resolve data errors and inconsistencies.
  • Prepare and manage the overall project budget throughout the life cycle of the project, taking overall responsibility for cost control, timelines and project quality.
  • Continually review the project contract in order to ensure that any out of scope work is managed promptly and efficiently.

  • Background in medicine, science or other relevant discipline and appropriate experience.
  • Candidate must have appropriate data management experience
  • Ability to manage all aspects of data management study management and solve problems independently.
  • Appropriate experience and understanding of at least one clinical data management system (e.g. Rave, Oracle Clinical, Clintrial) and a programming language (e.g. SQL, SAS).
  • Ability to successfully lead and manage project team(s).
  • Ability to liaise successfully with sponsors.
  • Ability and willingness to travel if required

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.

Are you a current ICON Employee? Please click here to apply: link


We offer a full range of consulting, clinical development and commercialisation services from a global network of offices in 46 countries

Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life.

We are a global provider of consulting, and outsourced development and commercialisation services to pharmaceutical, biotechnology, medical device and government and public health organisations. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas. ICON has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.

Find Us
01628 496300
3rd Floor
Marlow International
United Kingdom
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