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

• Develop and maintain collaborative working relationships with appropriate consultants and external experts for subject matter expertise and protocol development

• Compliant with departmental and broader organizational SOPs as fit for purpose, in compliance with current scientific standards and regulatory requirements

• Participate in project teams and serve as liaison to project teams, CRO's, Clinical sub-teams, and others

• Present data at scientific meetings, both internally and externally and author manuscripts in scientific journals

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

• Excellent written and oral communication skills

• Confidence and ability to present to and influence matrix teams and senior leaders

• Ability to work independently, manage multiple priorities, and thrive in a dynamic environment

• Genuine curiosity and drive to ask questions – looking for the ‘why’ of every project

• Experience in clinical pharmacology, immunology or oncology is preferred

• Early phase/Phase I experience required

• Willingness to travel up to 20%, accommodations available for individuals with disabilities

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 to read more about the benefits ICON offers.