•Manages clinical trial projects and ensures successful clinical trial planning, execution and delivery
•Ensures that clinical projects are delivered on time, within budget and aligned to the applicable quality standards
•Ability to drive trial start up by coordinating preparation of CPC by respective members and tracking
progress of start- up milestones (Feasibility, FPA, CPC, SIVs, FPFVs)
•Responsibility for regional recruitment at the study level, including responsibility for forecasting, setting
up contingency plans to ensure a target is achieved


•Scientific Bachelors’ or Masters’ degree in a relevant area
•Regional exposure as a CTM
•Indication specific expertise within oncology
•Excellent communication and organizational skills
•Business fluent in English