Proj Manager, Data Management

Project Manager Data Management - EU (Dublin, UK, Paris, Strasbourg, Madrid or Warsaw)

ICON Plc is a leading Clinical Research Organisation headquartered in Leopardstown, Dublin 18. Founded in Dublin in 1990 with a team of 5, ICON Plc now employs over 13,000 people in 38 countries.

The Role:

Due to new business wins, we are currently recruiting for a Project Manager to join the Data Management team in Europe. 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.

Responsibilities will include:

• Managing the Data Management team, study and/ or program of studies to ensure project objectives are met within budget and to agreed timelines.
• Proactively managing a team - supporting staff skills and encouraging growth.
• Develop and foster sponsor relationships through effective project management and communication.
• Contribute to the representation of data management on specific sponsor partnerships and/ or alliances by providing regular status reports and KPI's to senior Management.
• Manage the forecast and revenue recognition process by continuous review of monthly files to meet departmental objectives and profit and margins.
• Represent Data Management at internal and external audits and manage findings through resolution both operationally and within the quality management system.
• Provide project management to Biostatistics and Medical Writing when Clinical Operations is not a function provided by ICON.
• Lead the development, implementation and maintenance of guidelines and procedures to facilitate the efficient performance of data management activities.
• Lead and coordinate the design and implementation of departmental initiatives and training.
• Provide input into CRF design, protocol review, edit check specifications, data entry conventions, monitoring guidelines and any other study related documents as required.
• Actively participate in Business Development presentations to sponsors as required

The successful candidate will have:

• Degree in science.
• Experience working with some of the following systems: Rave, Inform, OCRDC, UX EDC etc.
• Proven in-depth clinical research industry experience.
• Experience managing and leading teams.
• Capability to manage completing priorities in a changeable environment.
• Experience working to tight deadlines.