Regulatory Submissions Manager

ICON Clinical Research, LP

Not specified; not specified; competitive salary m...
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Regulatory affairs experience in pharmaceutical industry
Experience with cta ind maa submissions
Ability to lead internal teams independently
** ICON Clinical Research is seeking a Regulatory Submissions Manager to lead regulatory activities and submissions within their Regulatory Affairs team. The ideal candidate will have a strong background in regulatory affairs, particularly with drug development submissions, and possess the ability to work independently and collaboratively. ICON offers a competitive benefits package and fosters an inclusive workplace culture. **

Job Summary

  • ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Manager of Regulatory Affairs to join their diverse team.
  • The role involves leading regulatory activities and submissions independently while providing guidance across various stages of drug development.
  • ICON offers competitive benefits including health insurance, retirement planning, and a global Employee Assistance Programme focused on well-being.

Matching Summary

Match Score: 75

** ICON Clinical Research is seeking a Regulatory Submissions Manager to lead regulatory activities and submissions within their Regulatory Affairs team. The ideal candidate will have a strong background in regulatory affairs, particularly with drug development submissions, and possess the ability to work independently and collaboratively. ICON offers a competitive benefits package and fosters an inclusive workplace culture. **

Salary

Not specified; Not specified; Competitive salary mentioned

Skills & Requirements

Must-have

  • Regulatory affairs experience in pharmaceutical industry
  • Experience with CTA IND MAA submissions
  • Ability to lead internal teams independently
  • Strong understanding of global regulatory requirements

Nice-to-have

  • Advanced degree in scientific or healthcare field
  • Experience in early drug development stages
  • Collaborative cross-functional team member

Key Requirements

  • Bachelor's degree in scientific or healthcare-related field
  • Minimum 6 years of experience in regulatory affairs
  • Prior experience with CTA/IND/MAA submissions

Work Rights

Not specified

Tailored Resume

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