Global Site Activation Manager, Europe

IQVIA Argentina; Reading; Remote; GBP 40,000 - 80,000; Full time

Job summary

Join a leading global team in Clinical Trial Site Activation as a Global Site Activation Manager. This role offers the opportunity to manage the Start-Up phase of clinical trials, ensuring effective strategy implementation and timely project delivery. You will collaborate with various project team members and utilize advanced regulatory intelligence systems to drive success. This innovative firm provides a remote work environment and vast career growth opportunities, making it an exciting chance to advance your career in clinical research and project management.

Qualifications

• 5+ years in clinical research with 2+ years overseeing global studies.
• Experience in project management, budget control, and regulatory processes.

Responsibilities

• Manage the Start-Up phase of clinical trial site activation.
• Oversee country operations teams to ensure timely delivery of client commitments.

Skills

Project Management

Clinical Research

Regulatory Knowledge

Budget Control

Education

Bachelor's Degree in Life Sciences

Master's Degree in Life Sciences

Ph.D in Life Sciences

Job description

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

1. Bachelor's Degree, Master's Degree, or Ph.D in Life Sciences or a closely related field.
2. At least 5 years of experience within the clinical research space with a minimum of 2+ years of experience overseeing global clinical studies.
3. Project ownership controlling delivery on time, within scope, and controlling budget.

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