The candidate will work in close collaboration with the Head of PPMO, the Senior PMs and the other members of the PPMO team to manage R&D projects of multiple levels of complexity, from early (IND ready to Ph1-2) to later stages (Ph3 and beyond) of the Clinical Drug Development and Life Cycle Management.
Responsibilities
Establish and maintain project and operational documentation (Agenda, Meeting Minutes, Gantt Chart, Project Trackers, Stakeholder Chart, Risk Management Tool, communication grid, etc.)
Qualifications
Ability to understand and integrate / manage data from various sources in the context of clinical trials in Oncology.
J-18808-Ljbffr