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Data Management, Project Manager

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About the role

This vacancy has now expired. Please click here to view live vacancies.

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. The Project Manager will be responsible for managing data management teams, studies and programs of studies under the general direction of the Associate Director/Director of Data Management.
  
Overview of the Role
  • Manage the Data Management team, study and or program of studies to ensure project objectives are met within budget, to agreed timeline and to high level of quality; clinical data management staff as appropriate, including but not limited to resource planning, recruitment, performance evaluations and training.
  • Develop and foster sponsor relationships through effective project management and communication.
  • Provide regular status reports and KPIs to senior management and represent Data Management at oversight meetings. Manage the forecast and revenue recognition process by continuous review of monthly files and incremental review of project analysis files to meet departmental objectives for profit and margins.
  • Represent Data Management at internal/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. Contribute to the development, implementation and maintenance of guidelines and procedures (SOPs, training manuals, etc.) to facilitate the efficient performance of data management activities.
Role Requirements / Skills / Experience Required 
  • Bachelor’s degree or local equivalent in a scientific discipline is required
  • A minimum of 6 years clinical data management experience and at least 1 year of supervisory experience (including project management, resource planning, staff recruitment, performance evaluations, career development and training). Knowledge of FDA regulations and all relevant local or regional regulations respecting data quality and clinical trials conduct
  • Appropriate experience and understanding of at least one clinical data management system (e.g. RAVE, INFORM, OCRDC)
  • Travel (approximately 15%) domestic and/or international  
What’s Next
Following your application if you are successful you will be invited to an initial telephone interview with one of our dedicated recruiters who will be able to provide you with more details of this opportunity.
 
ICON is an equal opportunity employer - M/F/D/V and committed to providing a workplace free of any discrimination or harassment
 
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