Job Description

Summary:
Reporting to the Chief Medical Officer and collaborating with external regulatory advisors, this role is responsible for developing and executing regulatory strategies from early development through late-stage clinical programs. The role involves direct interaction with the FDA and global regulatory agencies, leading submissions, and providing regulatory guidance across functional teams.

Key Responsibilities:

• Serve as the primary contact with FDA and other regulatory agencies, preparing for and leading agency meetings.
• Lead the preparation and submission of domestic and global regulatory documents (e.g., IND, CTA, NDA/MAA) and manage response strategies to regulatory inquiries.
• Prepare and maintain regulatory submissions, ensuring compliance with FDA and global health authority requirements.
• Provide interpretation, guidance, and training on global regulations to internal teams, identifying regulatory opportunities and risks.
• Pursue special and expedited review designations as appropriate for development programs.

Qualifications:

• Bachelor's degree in a relevant field; advanced degree preferred.
• 10+ years of experience in the pharmaceutical/biotechnology industry, with at least 5 years in Regulatory Affairs.
• Experience in key areas of regulatory affairs, including strategy development, global submissions, agency meetings, and expedited designations; CMC experience is a plus.
• Experience in ophthalmology is an advantage.
• Project management experience is beneficial.
• Strong oral and written communication skills.
• Comprehensive understanding of global pharmaceutical development, including clinical and nonclinical activities.

Department: Direct Clients
This is a full time position

Job Tags

Full time,

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