# Senior Global Regulatory Scientist

**Company**: ICON
**Work arrangement**: remote
**Experience**: senior
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Mexico-Mexico-City/Senior-Global-Regulatory-Scientist_JR155892?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
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## Description

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 Senior Global Regulatory Scientist at ICON, you will provide high-level regulatory and scientific expertise to support global development strategies and submissions.

**Responsibilities:**

- 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 a relevant scientific discipline or healthcare-related field

- Extensive 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 written and verbal communication abilities, with meticulous attention to detail.

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

- Willingness to travel as required (approximately 10%)

**Rewards & Benefits**

- 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

## Skills

### Required
- regulatory affairs
- global clinical development regulations
- FDA
- EMA
- ICH
- scientific writing
- communication
- analytical skills
- critical thinking

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