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Design and implement clinical trial protocols, analyze and interpret study data, and collaborate with cross-functional teams to support effective study execution and data quality. Communicate findings to stakeholders and contribute to regulatory submissions, study reports, and scientific publications.
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 Clinical Scientist at ICON, you will design and conduct clinical studies that advance our understanding of new therapies.
What You Will Do:
You will take responsibility for clinical research deliverables, applying your skills to ensure quality and efficiency.
Key responsibilities include:
Your Profile:
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:
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:
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
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