The IQVIA Global Site Activation team is one of the clear market leaders in Clinical Trial Site Activation, driving best in class employee, site and customer experiences. This position can be anywhere in Europe, remote.
Job Overview
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 oversee 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, 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.
Qualifications
Bachelor's Degree, Master's Degree, or Ph.D in Life Sciences or a closely related field.
At least 5 years of experience within the clinical research space with a minimum of 2+ years of experience overseeing global clinical studies.
Project ownership controlling delivery on time, within scope, and controlling budget.
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