Senior Global Regulatory Scientist

Homebased role

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a Senior Global Regulatory Scientist to join our diverse and dynamic team. As a Senior Global Regulatory Scientist at ICON, you will provide high-level regulatory and scientific expertise to support global development strategies and submissions. You will collaborate with sponsors and cross-functional teams to navigate complex regulatory pathways and enable successful product development.

What You Will Be Doing:

Leading the development of global regulatory strategies for clinical programmes, including plans for key health authority interactions and milestones.

Authoring and reviewing complex regulatory documents such as clinical trial applications, briefing books, and major submission components.

Interpreting evolving global regulations, guidelines, and precedents, and advising teams on implications for programme design and execution.

Providing strategic input into clinical development plans, risk management strategies, and labelling considerations.

Representing regulatory functions in sponsor and health authority meetings, ensuring clear, scientifically robust communication.

Mentoring junior regulatory colleagues and contributing to internal best practices, templates, and knowledge-sharing initiatives.

Your Profile:

Bachelor's degree in life sciences, pharmacy, medicine, or a related discipline, or equivalent regulatory experience.

4+ years experience in regulatory affairs or regulatory science within pharma, biotech, or CRO environments.

Strong knowledge of global clinical development regulations (e.g., FDA, EMA, ICH) and regional requirements.

Excellent scientific, analytical, and critical-thinking skills, with the ability to integrate complex data into regulatory positions.

Outstanding English written and verbal communication abilities

Proven experience interacting with health authorities and leading cross-functional regulatory projects

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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised travel passes, health assessments, among others.

Visit our careers site to about the benefits ICON offers.

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request .

Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.

Are you a current ICON Employee?