ICON
Study Site Management Specialist
Poland, Warsaw
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hirly's read of this role
- Seniority
- Mid level
- Country
- PL
- Work mode
- On-site / unstated
- First seen by hirly
- 6 Oct 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
Site Activation Lead 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 benefit 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.
What You Will Do:
You will manage day-to-day site start-up and activation activities, supporting your team to deliver quality outcomes.
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.
#LI-MC1
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 5 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 deadlines and manage multiple priorities.
- Willingness to travel as required (approximately 15%)
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
Benefits may vary depending on role and location.
Visit our careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here .
Are you a current ICON Employee? Please click here to apply
Listed on hirly, a job board. hirly is not the employer: ICON is hiring for this role.
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