Regulatory Submissions Manager (EU CTR)

ICON plc

1 month ago

Paris, France

Hybrid

Full Time

Senior

0 applicants

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About this role

The Regulatory Submissions Manager at ICON is responsible for managing regulatory activities related to drug development, including submissions and agency interactions in the EU and UK. They provide regulatory guidance and support across various stages of development, helping to ensure compliance with global regulatory requirements.

Skills

Qualifications

Bachelor's Degree in a Scientific or Healthcare-related Field

About ICON plc

iconplc.com

ICON plc is a global clinical research organisation (CRO) that provides outsourced clinical development and commercialisation services to pharmaceutical, biotechnology and medical device companies. It offers end-to-end drug and device development support — including clinical trial management across phases, data management and biostatistics, regulatory and safety/pharmacovigilance, and commercialisation and market-access services. ICON combines scientific and therapeutic expertise with technology and a scalable global operations network to accelerate development and bring therapies to patients. Clients engage ICON for integrated, experienced CRO support across the full product lifecycle.