Site Activation Specialist
Pubblicato il 26-09-2026 - Iqvia in Milano
Site Activation SpecialistCountry Site Activation - CSAWork Location: Milan, Italy- Please note that attendance at our Milan office is mandatory at least two days per weekMake an impact on patient healthIQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. We keep the patient at the forefront; ‘Always Impatient for the Patient’ and we excel in our collaboration with our external/internal customers.IQVIA’s Country Site Activation team are a global network who identify and activate sites to the highest quality to ensure patients on Clinical trials have access to safe and effective medication. We are leaders in innovation and first to new technologies, meaning a vast amount of career development opportunities are available.Job Overview:As a Site Activation Specialist, you will serve as a Single Point of Contact to perform feasibility, site activation and some maintenance activities in assigned studies for investigative sites, according to applicable regulations, SOPs and work instructions,
working closely with the Site Activation Manager, Project Management team, and other departments as necessary.You will review documents for completeness, consistency, and accuracy, under guidance of senior staff and prepare site documents, inform team members of completion of regulatory contracts. Along with distributing completed documents to sites and internal project team member and updating and maintaining internal systems, databases, tracking tools, timelines, and project plans with accurate and complete project specific information.You will also review, track, and follow up the progress, the approval and execution of required documents such as questionnaires, CDAs, regulatory, ethics, Informed Consent Form, and Investigator Pack release documents.Requirements and Skills : Bachelor’s Degree in Life Science2 - 3 years’ prior experience in clinical research / site activationExperience of regulatory