Senior Clinical Scientist
ICON 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 Senior Clinical Scientist at ICON, you will design and conduct clinical studies that evaluate the safety and efficacy of innovative treatments.

What You Will Do:

• Provide strategic leadership and demonstrating accountability for the clinical programs supporting early clinical development and clinical pharmacology
• Maintain updated knowledge of competitive landscape on current assets or evolving standards of care for indications of interest and provide subject matter expertise on cross-functional project teams
• Author/Review/Approve clinical protocols, analysis plans, study reports and regulatory submissions in collaboration with physicians, statisticians and other critical functions.
• Execute Clinical & Clinical Pharmacology studies in close collaboration with Clinical Operations
• Review and summarize clinical safety or efficacy data in collaboration with the Medical Monitor
• Work closely with Quantitative Clinical Pharmacology, Translational Sciences and Statistics to develop protocols and summarize analysis
• Contribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans
• Draft and review of clinical scientific documents such as IND, IND amendments, Investigator Brochures, Annual Reports and other Health Authority submissions
• Ensure adherence to agreed timelines and budgets to ensure prompt and accurate execution of deliverables from clinical studies and programs

Your Profile:

• At least 5 years’ experience and a, PhD, PharmD or MD degree or at least 10 years’ experience with BS/MS degree with emphasis on early development, clinical pharmacology or a related discipline
• Ability to critically analyze problems and provide creative solutions
• Experience in clinical pharmacology, immunology or oncology is preferred
• Early phase/Phase I experience required

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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

About Us
ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live.

If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry.

ICON is an equal opportunity employer.