09 ott - Roma
Altro
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As the world's largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that vantaggi patients worldwide.
As a Site Activation Lead at ICON, you will advance clinical trial start-up activities by understanding client objectives and assist in the development of the plan for country and site distribution.
You will manage day-to-day site start-up and activation activities, supporting your team to deliver quality outcomes.
What You Will Do
Key Responsibilities Include
Lead clinical trial start-up activities, understanding client objectives and assisting in the development of plans for country and site distribution.
Oversee day-to-day delivery of all aspects of site activation in assigned projects, ensuring adherence to sponsor timelines, expectations, and compliance with ICON/client KPIs, SOPs, and regulatory standards.
Ensure that each project has a comprehensive site activation plan, conducting studies effectively in accordance with the plan.
Lead sponsor initiatives such as kick-off meetings, bid defenses, project updates, status calls, and other key communications.
Utilize project management skills to optimize performance and collaboration, ensuring successful study outcomes.
Your Profile
You will have solid site start-up and activation experience, with the ability to manage competing priorities and develop your team.
Required Qualifications And Experience
Bachelor's Degree, preferably in life sciences.
Minimum of 4 years of experience in a Clinical Research environment, focusing on Start-Up experience.
Strong project management skills, with a deep understanding of regulatory and submission processes in various countries.
Excellent written and verbal communication abilities.
Proven ability to work efficiently to tight deadli
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