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Sr Proj Mgr, Data Management

Reference: 060368_1573833260

Senior Project Manager, Data Management

*Role can be based in Dublin, UK (London, Marlow or Eastleigh), Paris, Strasbourg, Madrid or Warsaw*
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 organizational goals.
  • 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

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