Regulatory Submissions Manager (EU CTR)

Clinical Careers Page(11 days ago)

HybridFull TimeSenior$75,000 - $95,000Regulatory Affairs

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.

View Original Listing

Required Skills

Regulatory Submissions
CTA
IND
MAA
EU CTR
UK Regulations
Regulatory Strategy
Drug Development
Agency Interaction
Clinical Trials

Qualifications

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

About Clinical Careers Page

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.

View more jobs at Clinical Careers Page →