Senior Global Regulatory Affairs Specialist
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Before you apply
LocationUK, Reading; Spain, Madrid; Poland, Warsaw; Bulgaria, Sofia; Ireland, Dublin
Work modeon-site
Typefull-time
SenioritySenior
Experience5+ yrs
Company size10,000+ people
PostedOct 23, 2026 · 2w ago
Verified live18h ago
At a glanceSummarised by Seekless from the posting.
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
Legal right to work in the country where the role is based
Benefits
Competitive base salary
Performance related incentives
Health insurance
Dental coverage
Vision coverage
Retirement plan
Life assurance
Disability coverage
Employee assistance program
Wellbeing resources
Learning and development opportunities
About the role
Senior Global Regulatory Affairs Specialist
About the company
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 values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
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.
What You Will Do:
You will take ownership of regulatory affairs deliverables, applying your expertise to complex challenges.
Key responsibilities include:
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Developing global regulatory strategies for the successful submission and approval of clinical trial applications and marketing authorizations.
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Providing regulatory guidance and support to cross-functional teams throughout the drug development process.
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Ensuring compliance with global regulatory requirements and standards.
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Managing regulatory submissions and interactions with health authorities.
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Participating in regulatory intelligence activities to stay updated on changes in regulations and guidelines.
Your Profile:
You will have a strong foundation in regulatory affairs, with the experience to work independently and guide others.
Required qualifications and experience:
•
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.
Legal
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 careers site to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.
Are you a current ICON Employee? Please click here to apply