21 set - Milano
Iqvia
Site Activation Specialist
Please note that attendance at our Milan office is mandatory at least two days per week
Make an impact on patient health
IQVIA’s Global Site Activation Team of 2000 employees, drives best in class site and customer experience, with industry leading outcomes. 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.
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.
Bachelor’s Degree in Life Science
~2 - 3 years’ prior experience in clinical research / site activation
~ Experience of regulatory submissions essential.
~ Good interpersonal, communication and organisational skills to establish and maintain effective working relationships with co-workers, managers and sponsors
~ Ability to work on multiple projects
~ Knowledge of applicable functional/regulatory requirements, including local regulations, SOPs and ICH/ GCP
~ Distribut
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