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Job Description & How to Apply Below
Elevate your career with Allucent as the Vice President of Regulatory Affairs. This hybrid/remote opportunity focuses on regulatory guidance for drug and medical device products while leading a dedicated team.
Allucent is seeking a Vice President of Regulatory Affairs to join its A-team. In this pivotal role, you will manage regulatory activities, directly assist clients in navigating submissions, and oversee Health Authority interactions. Your expertise will help shape project directions, ensuring timely and valid regulatory compliance in both the US and Canada.
Key Responsibilities:
• Lead regulatory team and client management activities
• Oversee Health Authority communications and submissions
• Assist in translating regulatory requirements into actionable plans
• Serve as Subject Matter Expert or Project Lead in teams
• Provide counsel on drug, biologic, or medical device projects
Requirements:
• Degree in scientific area (B.Sc., M.Sc., Ph.D.)
• Advanced regulatory knowledge for US, EU, and Canada
• RAC credentials preferred
• Experience in drug or device development
• Strong analytical and communication skills
Utilize your leadership and regulatory expertise to drive impactful results in Allucent’s innovative environment.
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