This position is responsible for the execution of a clinical development program from protocol
design to the final clinical study report for one or several studies.  This also includes
managing the process and people involved either as direct reports or though matrix reporting
via the clinical indication team.  The position is responsible for coordinating all efforts for
the trial both within CTI and through a wide variety of vendors.  Other responsibilities
include: driving all aspects of the project management process from initiation, planning,
execution, control and closure, planning and directing timelines, creating project budgets and
managing cost to budgets.   This position has overall responsibility to deliver the projects on
time and on budget.  Requires a Bachelor�s degree with at least 8 years of pharmaceutical
clinical development experience or equivalent.  Must have experience with Phase I-III trials,
CRO management and project and contract management.  An advanced degree (Master�s or PhD),
oncology/hematology clinical trial experience, NDA filing experience, international clinical
development experience and/or 10+ years of applicable experience is preferred.  Project
Management Certification (PMP) a plus