10 set - Milano
Icon Clinical
Global Study ManagerICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Clinical Trial Manager at ICON, you will manage clinical trial operations activities on a global level, supporting your global team and stakeholders to deliver high-quality outcomes across our clinical programmes and feeding into the Global Project Manager.
What You Will Do:
You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes at a study management levelKey responsibilities include: Plan and manage all aspects of clinical trials, ensuring adherence to timelines, vendor budget, and quality standards.
Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures.
Build and manage strong relationships with global stakeholdersVendor management
La preghiamo di leggere attentamente la seguente descrizione del lavoro per assicurarsi di essere la persona giusta per questo ruolo prima di candidarsi.
- setting up vendors, leading vendor calls for their performance and KPIs as well as managing vendor budgetsEnsure all trials are conducted in compliance with local, national, and international regulations and ethical guidelines.
Problem-solve and make critical decisions regarding trial design, vendor selection, and risk management.
Your Profile:
You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.
Required qualifications and experience: University degree in medicine, science, or equivalent combination of education & experienceMinimum of 5 years in Clinical Research industry working within a Pharma or CROMust have vendor management experience includi
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