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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 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.

Qualifications

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.

Project ownership controlling delivery on time, within scope and controlling budget.

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IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com