Executive Director, Regulatory Affairs Liaison

Scorpion Therapeutics; North Wales (Montgomery County); Hybrid; USD 180,000 - 240,000; Full time

Benefits offered by this job

Hybrid work arrangement

Up to 10% travel

Job summary

Scorpion Therapeutics seeks an Executive Director of Regulatory Affairs Liaison in General Medicine to lead global regulatory strategy for ophthalmology programs, with oversight of retinal disease indications and external representation.

The role requires extensive drug development and regulatory leadership experience, including NDA/BLA submissions, and a proven track record of delivering regulatory milestones in a hybrid work environment.

Qualifications

• 12+ years drug development experience (or 9+ with MD/PhD/PharmD).
• 7+ years in regulatory affairs.
• Proven NDA/BLA approvals.
• Strong communication and leadership skills.

Responsibilities

• Develop and oversee global regulatory plans for retinal disease indications.
• Manage and mentor a team of Global Regulatory Leads.
• Ensure regulatory deliverables (submissions, labels, study protocols) meet objectives.
• Represent the company externally in regulatory matters.

Skills

Strong communication

Leadership

Education

B.S./M.S. in related field

MD/PhD/PharmD

Job description

Role:

Executive Director, Regulatory Affairs Liaison in General Medicine, leading global regulatory strategy for ophthalmology programs.

Responsibilities:

develop and oversee global regulatory plans for retinal disease indications, manage and mentor a team of Global Regulatory Leads, ensure regulatory deliverables (submissions, labels, study protocols) meet objectives, and represent the company externally in regulatory matters.

Qualifications:

B.S./M.S. with 12+ years or MD/PhD/PharmD with 9+ years drug development experience, including at least 7 years in regulatory affairs; proven success in NDA/BLA approvals; strong communication and leadership skills.

High-Value:

ophthalmology and retinal disease programs, U.S. and global regulatory scope, 10% travel, hybrid work setup.

Preferred:

experience in retinal therapy, large/molecule programs, global regulatory leadership, and team management.