As a Global Site Activation Manager you will be our project manager for the Start-Up phase, in charge of the design and implementation of our strategy towards sites activation from award until open to enrolment. You will also oversees our country operations teams ensuring that our client commitments are delivered timely and according to project scope and processes.

The key project team members that the SAM interacts with are; the project manager, the clinical lead, a regulatory and contract and budget solution advisors and the country regulatory specialists. The SAM also counts on a rich regulatory intelligence database and best in class systems to enable the start up strategy execution.

The Site Activation Manager is a fundamental role to deliver our clinical trial portfolio and belongs to a global unit with vast career growth opportunities.

Bachelor's Degree, Master's Degree or Ph.D in Life sciences or a closely related field.

At least 5 years experience within the clinical research space with a minimum of 2+ years of experience overseeing global clinical studies.