VP, Regulatory Affairs

Scorpion Therapeutics; Wilmington (DE); On-site; USD 260,000 - 320,000; Full time

Job summary

Scorpion Therapeutics seeks a Vice President of Regulatory Affairs to provide strategic and operational oversight of regulatory activities across biopharma product development. You will develop and execute regulatory strategies, ensure compliance, and manage submission plans from preclinical through post-approval stages.

The role involves leading a regulatory team, guiding cross-functional groups, and preparing for FDA and global authority meetings.

Qualifications

• PhD or master's degree with relevant experience.
• 15+ years in regulatory affairs within biopharma, with expertise in drug development processes, global regulations, and CMC considerations.
• Preferred skills include knowledge of small molecule regulations, international submissions, and familiarity with Chinese regulations.

Responsibilities

• Leading a regulatory team
• Guiding cross-functional groups
• Preparing for FDA and global authority meetings
• Managing regulatory filings (e.g., INDs, BLAs, NDAs)
• Maintaining regulatory intelligence on global standards
• Direct interaction with regulatory agencies
• Representing regulatory interests in leadership forums
• Managing risk communication

Skills

Regulatory leadership

Cross-functional collaboration

Regulatory submissions

Regulatory strategy

Education

PhD or Master’s degree in a relevant field

Job description

Role: Vice President of Regulatory Affairs responsible for strategic and operational oversight of regulatory activities in biopharma product development. Objectives include developing and executing regulatory strategies, ensuring compliance, and managing submission plans for preclinical, clinical, and post-approval stages.

Responsibilities

• Leading a regulatory team
• Guiding cross-functional groups
• Preparing for FDA and global authority meetings
• Managing regulatory filings (e.g., INDs, BLAs, NDAs)
• Maintaining regulatory intelligence on global standards
• Direct interaction with regulatory agencies
• Representing regulatory interests in leadership forums
• Managing risk communication

Qualifications

• PhD or master's degree with relevant experience
• 15+ years in regulatory affairs within biopharma, with expertise in drug development processes, global regulations, and CMC considerations
• Preferred skills include knowledge of small molecule regulations, international submissions, and familiarity with Chinese regulations

High-Value: leadership in regulatory strategy, extensive industry experience, global regulatory knowledge, expertise in pharmaceutical development and manufacturing.

Work setup and travel requirements are not specified.