clinical scientist
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Before you apply
LocationUS, Blue Bell (ICON); Canada, Burlington
Work moderemote · United States
SeniorityMid
Company size10,000+ people
PostedNov 2, 2026 · 2d ago
Verified live1d ago
At a glanceSummarised by Seekless from the posting.
Bachelor's degree in a relevant scientific discipline or healthcare-related field
Experience in clinical research or a related scientific role, with a strong understanding of clinical trial processes
Excellent analytical skills and proficiency in data interpretation and statistical analysis
Strong communication and collaboration skills, with the ability to work effectively in interdisciplinary teams
Detail-oriented and committed to maintaining high standards of data integrity and quality
Willingness to travel as required (approximately 20%)
Legal right to work in country where role is based
Benefits
Health insurance
Dental coverage
Vision coverage
Retirement plan
Life insurance
Disability coverage
About the role
Clinical Scientist
About the company
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:
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Designing and implementing clinical trial protocols, ensuring adherence to scientific and regulatory standards.
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Conducting data analysis and interpretation to derive insights that support study objectives.
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Collaborating with cross-functional teams to ensure effective study execution and data quality.
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Engaging with stakeholders to communicate findings and contribute to scientific discussions.
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Assisting in the preparation of regulatory submissions, study reports, and scientific publications.
Your Profile:
You will bring relevant clinical research experience, along with the following qualifications and skills.
Required qualifications and experience:
•
Bachelor’s degree in a relevant scientific discipline or healthcare-related field
•
Experience in clinical research or a related scientific role, with a strong understanding of clinical trial processes.
•
Excellent analytical skills and proficiency in data interpretation and statistical analysis.
•
Strong communication and collaboration skills, with the ability to work effectively in interdisciplinary teams.
•
Detail-oriented and committed to maintaining high standards of data integrity and quality.
•
Willingness to travel as required (approximately 20%)
Legal
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:
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Competitive base salary and performance related incentives
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Health and wellbeing programmes including medical, dental, and vision coverage where applicable
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Retirement and pension plans
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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.