.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, France, Portugal or UKThis 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.Role: Manage and Develop Team CapabilityOversee 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.Manage and appraise all staff under jurisdiction.Deliver Project to Quality, Timeline and Budget RequirementsPlan, 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.Requirements Background in medicine, science or other relevant discipline and appropriate 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
