Director, Regulatory Affairs

Clinical Careers Page(1 month ago)

RemoteFull TimeDirector$222,600 - $295,268 (estimated)Regulatory Affairs

About this role

A Director, Regulatory Affairs at ICON is a senior leader within the Regulatory Consulting Solutions team providing high-level regulatory expertise for global clients, with emphasis on Europe and the UK. The role represents ICON as a subject matter expert across drug development through post‑marketing and supports business growth through strategic client engagement and thought leadership. This is a remote role based in the EU or UK.

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Required Skills

Regulatory Strategy
Health Authorities
Dossier Preparation
Regulatory Writing
Clinical Development
Client Engagement
Project Management
Team Leadership
EMA Interactions
Lifecycle Management

+2 more

Qualifications

Bachelor's Degree
MSc
PhD
M.D.
Pharm.D.
MBA

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.

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