# Regulatory Scientist

**Company**: ICON
**Location**: Buenos Aires, Argentina
**Job type**: full-time
**Category**: Healthcare
**Industry**: Healthcare

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/Argentina-Buenos-Aires/Regulatory-Scientist_JR161625?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/job/regulatory-scientist-51cf122b-e70/

## 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 Regulatory Scientist at ICON, you will support the development, implementation, and execution of regulatory strategies for clinical development programs.

**Responsibilities**

- Preparing, reviewing, and coordinating regulatory documents such as clinical trial applications, briefing packages, and responses to health authority questions.

- Contributing to regulatory strategy development for clinical programs, including plans for health authority interactions and submissions.

- Interpreting and applying relevant regulations, guidelines, and precedents to support compliant study design and execution.

- Collaborating with clinical, safety, CMC, and other cross-functional teams to ensure alignment of regulatory content and messaging.

- Monitoring changes in the regulatory environment and providing guidance on potential impact to programs and submissions.

- Supporting regulatory interactions and meetings, including preparation of materials and documentation of outcomes.

**Your Profile**

- Bachelor's degree in a relevant scientific discipline or healthcare-related field

- Experience in regulatory affairs, regulatory writing, or clinical development within the pharma, biotech, or CRO industry.

- Good understanding of global regulatory frameworks and guidelines relevant to clinical development.

- Strong scientific, analytical, and critical thinking skills, with the ability to interpret complex data and regulations.

- Excellent English - written and verbal communication skills, with high attention to detail and accuracy.

- Ability to work effectively in cross-functional teams and manage multiple regulatory activities and timelines.

**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

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## Skills

### Required
- regulatory affairs
- regulatory writing
- clinical development
- global regulatory frameworks
- English

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