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- Tasks: Lead regulatory tasks for clinical trials across Europe, ensuring compliance and quality.
- Company: Join ICON plc, a top-tier healthcare intelligence and clinical research organisation.
- Benefits: Enjoy competitive salary, health insurance, flexible benefits, and a supportive work culture.
- Why this job: Shape the future of clinical development in an inclusive environment that values innovation.
- Qualifications: 3+ years of regulatory experience; fluent in English; strong communication skills.
- Other info: Willingness to travel less than 5%; training and mentoring opportunities available.
The predicted salary is between 36000 - 60000 £ per year.
Senior Regulatory Scientist – UK based
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.
As a Senior Regulatory Scientist, you will primarily work with the ICON Clinical Trial Units in the Netherlands and Hungary. Your responsibilities include completing country-specific Clinical Trial Regulatory deliverables according to study specifics, ICON policies, procedures, applicable regulations, and ICH-GCP principles, with sound scientific/technical foundations. Depending on experience, you may also be involved in staff training/mentoring and contributing to the review of ICON systems and procedures.
Minimum requirements:
- At least 3 years of relevant regulatory experience
- Fluent in reading, writing, and speaking English
- Willing to travel less than 5%
- Commitment to ICON\’s values centered around People, Clients, and Performance
- Ability to contribute to process improvements and streamline workflows
- Experience ensuring regulatory deliverables comply with relevant regulations, guidelines, policies, and procedures within timelines and budgets
- Experience interacting with regulatory authorities and other country-level bodies
- Ability to coordinate and prepare submission documentation accurately and timely
- Experience managing submissions through lifecycle to approval
- Effective communication with project teams regarding regulatory status
- Completion of project-specific training as required
- Ability to manage budgets and identify out-of-scope activities
What ICON can offer you:
Our success depends on the quality of our people. We’ve built a diverse culture that rewards high performance and nurtures talent.
- Competitive salary and benefits tailored to each country
- Annual leave entitlements
- Health insurance options
- Retirement planning options
- Global Employee Assistance Programme, LifeWorks
- Life assurance
- Flexible benefits such as childcare vouchers, gym discounts, and travel passes
Visit our careers site to learn more about ICON’s benefits.
At ICON, inclusion & belonging are fundamental. We are committed to providing an inclusive, accessible environment free of discrimination and harassment. All qualified applicants will receive equal consideration regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
If you need a reasonable accommodation during the application process or to perform the job, please let us know or submit a request here.
Interested but unsure if you meet all requirements? We encourage you to apply — you might be exactly what we’re looking for.
Current ICON employee? Please click here to apply.
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Senior Regulatory Scientist employer: ICON plc
Contact Detail:
ICON plc Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Regulatory Scientist
✨Tip Number 1
Familiarise yourself with the specific regulations and guidelines relevant to clinical trials in the UK and Europe. Understanding ICH-GCP principles and how they apply to ICON's operations will give you a solid foundation to discuss during interviews.
✨Tip Number 2
Network with professionals in the regulatory field, especially those who have experience with ICON or similar organisations. Engaging with them on platforms like LinkedIn can provide insights into the company culture and expectations for the role.
✨Tip Number 3
Prepare to discuss your experience with managing submissions and interacting with regulatory authorities. Be ready to share specific examples of how you've ensured compliance and streamlined processes in your previous roles.
✨Tip Number 4
Showcase your commitment to continuous improvement and process optimisation. Think of instances where you've contributed to enhancing workflows or training others, as this aligns well with ICON's values and mission.
We think you need these skills to ace Senior Regulatory Scientist
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights your relevant regulatory experience, especially any roles that involved clinical trials or interactions with regulatory authorities. Use keywords from the job description to demonstrate your fit for the Senior Regulatory Scientist position.
Craft a Compelling Cover Letter: In your cover letter, express your enthusiasm for the role and the company. Mention specific experiences that align with the responsibilities outlined in the job description, such as managing submissions or contributing to process improvements.
Showcase Communication Skills: Since effective communication is crucial for this role, provide examples in your application of how you've successfully communicated with project teams or regulatory bodies in the past. This could be in your CV or cover letter.
Highlight Continuous Learning: Mention any relevant training or certifications you have completed, especially those related to regulatory affairs or clinical research. This shows your commitment to staying updated in the field and aligns with ICON's values of innovation and excellence.
How to prepare for a job interview at ICON plc
✨Understand Regulatory Frameworks
Familiarise yourself with the specific regulations and guidelines relevant to clinical trials, especially ICH-GCP principles. Being able to discuss these frameworks confidently will demonstrate your expertise and commitment to compliance.
✨Showcase Your Experience
Prepare to discuss your previous regulatory experience in detail. Highlight specific projects where you successfully managed submissions or interacted with regulatory authorities, as this will illustrate your capability for the role.
✨Emphasise Communication Skills
Effective communication is key in this role. Be ready to provide examples of how you've communicated regulatory statuses to project teams or trained staff, showcasing your ability to convey complex information clearly.
✨Demonstrate Problem-Solving Abilities
Think of instances where you've contributed to process improvements or streamlined workflows. Discussing these experiences will show your proactive approach and ability to enhance efficiency within regulatory processes.