As a Clinical Project Manager (PM) you will thrive in a fast-paced environment where you will be responsible for leading one or more clinical trials simultaneously and be responsible for end-to-end project management activities including initiation, conduct, tracking and reporting of clinical trials. You will be responsible for coordination of the project team ensuring the study is delivered within budget, within the timelines and on target according to the requirements of the study specific contract.
The ideal candidate should have a bachelor’s degree (higher or equivalent) in a life science discipline with a significant track record within clinical project management, preferably on a global basis. They must possess excellent knowledge of the pharmaceutical product development process and have broad therapeutic area exposure. In addition, a strong commercial business awareness is a must.
The candidate must have excellent communication skills, in both English and French, with the ability to interact with senior managers and clients at all levels in order to develop key relationships.