Data Management Project Leader- North Wales, PA

The selected candidate will be the primary contact with the sponsor and will be responsible for the management of project activities and resources, staff evaluations and training, and project documentation. In this role, you will write study specific procedures, alert sponsors of any issues, plan and allocate sources and ensure that the project is going as planned according to the timeline. Additionally, you will be involved with ongoing set-up and closing.

Candidates should have a degree in the life sciences and/or relevant experience along with 3+ years of clinical-related data management experience in either a CRO or pharmaceutical company and have prior experience in managing and leading studies simultaneously. The ability to take leadership for the conduct of Data Management projects is required. Must be detail-oriented, able to multi-task, and possess excellent communication skills.

ICON Clinical Research is an Equal Opportunity Employer committed to strength in diversity.