Ra Cmc Consultant

ICON Clinical Research, LP

Ra cmc expertise
Global regulatory requirements
Drug development stages
As a Senior Manager, Regulatory Affairs at ICON, you will work closely with our client to provide them the RA CMC support that they need

Job Summary

  • As a Senior Manager, Regulatory Affairs at ICON, you will work closely with our client to provide them the RA CMC support that they need.
  • Be involved in the regulatory affairs activities across the ICON portfolio and be an expert and advisor to ICON clients (externally and internally).
  • ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities for you and your family.

Matching Summary

As a Senior Manager, Regulatory Affairs at ICON, you will work closely with our client to provide them the RA CMC support that they need.

Skills & Requirements

Must-have

  • RA CMC expertise
  • Global regulatory requirements
  • Drug development stages
  • Client advisory
  • Business development

Nice-to-have

  • Peptides and proteins experience
  • Module 3 CTD authoring

Key Requirements

  • Minimum of 7 years’ experience
  • Supervisory experience
  • Pharmaceutical/CRO industry experience
  • Development of regulatory strategies
  • Direct regulatory agency interaction

Work Rights

Not specified

Tailored Resume

Cover Letter