Senior Clinical Scientist - single client dedicated

What ICON can offer you:
Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family's needs.
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family's well-being.
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.

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• 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

• Early phase/Phase I experience required

• Experience in clinical pharmacology, immunology or oncology is preferred

Senior Clinical Scientist

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

• 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