Global Regulatory Scientist/Senior Global Regulatory Scientist
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 Integral Regulatory Scientist at ICON, you will prepare strategy and coordinate global clinical trial regulatory deliverables in compliance with ICON policies, applicable regulations, and ICH-GCP principles.
What You Will Do:
You will contribute to regulatory affairs activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
- Develop and implement global clinical trial submission strategies and regulatory plans in collaboration with stakeholders.
- Prepare, review, and finalize core documentation and ensure compliance with regulatory requirements.
- Coordinate submissions to regulatory agencies, ethics committees, and country-level authorities.
- Track and report submission progress in ICON systems,
ensuring accuracy and completeness of documentation.
- Represent Regulatory during audits, CAPAs, and client meetings, providing strategic input and solutions.
Your Profile:
You will bring relevant regulatory affairs experience, along with the following qualifications and skills.
Required qualifications and experience:
- Bachelor's degree and 0-3 years of relevant regulatory submission experience.
- Strong understanding of ICH-GCP and global regulatory guidelines.
- Excellent organizational and communication skills with attention to detail.
- Willingness to travel as required (approximately 10%)
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What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are
📌 Global Regulatory Scientist (España)
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