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Regulatory Affairs Director

2 months ago

Toronto, Ontario, Canada EVERSANA Full time
Job Summary

We are seeking a highly experienced and skilled Regulatory Affairs professional to join our team at EVERSANA as a VP, Regulatory. This is a key leadership role that will be responsible for driving the strategic and operational aspects of our regulatory affairs function.

Key Responsibilities
  • Develop and implement regulatory strategies to support business development activities and client deliverables.
  • Manage client relationships and ensure effective communication with internal stakeholders.
  • Oversee the development and submission of regulatory documents, including Clinical Trial applications, New Drug Submissions, and Supplemental New Drug Submissions.
  • Collaborate with internal departments to deliver on shared projects and ensure effective communication within the team.
  • Stay up-to-date with regulatory requirements and industry trends to ensure compliance and identify opportunities for growth.
Requirements
  • Master's degree in a relevant field, such as pharmaceutical sciences or regulatory affairs.
  • At least 20 years of experience in various pharmaceutical roles in Canada, with a strong background in regulatory affairs.
  • Excellent interpersonal and intercultural communication skills, both written and verbal.
  • Strong leadership and management skills, with experience in leading cross-functional teams.
  • Ability to work in a fast-paced environment and prioritize multiple tasks and projects.
What We Offer
  • Competitive wages and benefits package.
  • Opportunities for professional growth and development.
  • A dynamic and collaborative work environment.
  • Flexible work arrangements, including remote work options.