A Biopharmaceutical client of ours is hiring a Vice President of Global Regulatory Affairs to be based in New Jersey. This person will report to the CEO/ Vice President of Global Clinical Development. 

Responsibilities 

• Oversee all regulatory activities for the company
• Manage and oversee a team of Regulatory Affairs Professionals across various levels
• Be responsible for strategy relating to the global approval of NCEs and biosimilars in different markets
• Identify and coordinate educational trainings as needed and provide pertinent information on regulatory topics 
• Work closely with management team to implement short and long-term business plans and goals
• Build a connected and collaborative department to keep up with the growth and evolution of the company

Requirements

• 15 years of pharmaceutical/biotech experience in Regulatory Affairs
• Extensive knowledge of US and EU regulations
• Experience with a variety of regulatory submissions and regulatory agencies
• 5 years of experience supervising staff in the regulatory area

Key Skills

• Ability to work independently
• Superb oral communication and written skills 
• Demonstrated ability to manage multiple projects, lead people in a productive manner, and develop positive relationships. 

If this role is of interest to you, please send your CV to Marissa at m.saunders@hamlynwilliams.com to apply.