Senior Manager, Regulatory Affairs

ICON plc

Canada
Not specified
Health canada environmental regulations
New substance notification (nsn) submissions
Regulatory strategy development
ICON plc is seeking a Senior Manager in Regulatory Affairs to support clinical trials and registration applications in Canada. The ideal candidate will possess significant regulatory experience in the pharmaceutical or CRO industry, with strong organizational and communication skills

Job Summary

  • As a Senior Manager, Regulatory Affairs at ICON, you will play a pivotal role in supporting clinical trials and registration applications by assessing and preparing Environmental submissions for Canada and contributing to the advancement of innovative treatments and therapies.
  • 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.
  • At ICON, inclusion & belonging are fundamental to our culture and values, and we are dedicated to providing an inclusive and accessible environment for all candidates.

Matching Summary

Match Score: 85

ICON plc is seeking a Senior Manager in Regulatory Affairs to support clinical trials and registration applications in Canada. The ideal candidate will possess significant regulatory experience in the pharmaceutical or CRO industry, with strong organizational and communication skills.

Skills & Requirements

Must-have

  • Health Canada Environmental regulations
  • New Substance Notification (NSN) submissions
  • regulatory strategy development
  • document writing
  • marketing authorization applications
  • clinical trials support
  • direct regulatory agency interaction

Nice-to-have

  • foster an inclusive environment
  • driving innovation and excellence
  • trusted partner
  • business development activities
  • problem-solving ability
  • strong interpersonal skills

Key Requirements

  • Minimum of 7 years’ experience
  • supervisory experience
  • pharmaceutical/CRO industry experience
  • EU/APAC: In-depth proven regulatory affairs expertise
  • US/LATAM/CAN: Minimum of 6 years pharmaceutical/CRO industry
  • Demonstrable experience within regulatory affairs

Work Rights

Not specified

Tailored Resume

Cover Letter