# Senior Global Regulatory Affairs Specialist

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

**Apply**: https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Senior-Global-Regulatory-Affairs-Specialist_JR162485?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply
**Canonical**: https://yubhub.co/jobs/job_e1deedea-580

## 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 Affairs Specialist at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

**Responsibilities:**

- Developing global regulatory strategies for the successful submission and approval of clinical trial applications and marketing authorizations.

- Providing regulatory guidance and support to cross-functional teams throughout the drug development process.

- Ensuring compliance with global regulatory requirements and standards.

- Managing regulatory submissions and interactions with health authorities.

- Participating in regulatory intelligence activities to stay updated on changes in regulations and guidelines.

**Your Profile:**

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

- Minimum of 5 years of experience in regulatory affairs within the pharmaceutical or biotechnology industry.

- Strong understanding of global regulatory requirements and guidelines.

- Excellent communication and social skills.

- Ability to work independently and collaboratively in a fast-paced environment.

**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
- clinical trials
- medical data analysis
- global regulatory requirements

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Source: [Apply at icon.wd3.myworkdayjobs.com](https://icon.wd3.myworkdayjobs.com/en-US/broadbean_external/job/UK-Reading/Senior-Global-Regulatory-Affairs-Specialist_JR162485?utm_source=yubhub.co&utm_medium=jobs_feed&utm_campaign=apply)