Susan Skinner

EXPERIENCE

Susan Skinner, 42 years in the pharmaceutical industry; 36 years in Drug Regulatory Affairs, and 6 years in Pharmaceutical Research and Development; Extensive experience in Chemistry, Manufacturing, and Controls regulatory strategy, preparation and organization of regulatory submissions, including New Drug Applications, Biologic License Applications, Abbreviated New Drug Applications, and Drug Master Files

WHY WERE YOU SELECTED FOR YOUR CURRENT ROLE AT SHEARIT, LLC

Provide regulatory affairs support for the project and coordinate activities between Shearit, LLC and the Food and Drug Administration

PROUDEST ACCOMPLISHMENT

Founder of Skinner Pharma Consulting, LLC; 25 years as owner and President

COMMUNITY INVOLVEMENT & PROFESSIONAL MEMBERSHIP

• Active member of Regulatory Affairs Professionals Society and North Carolina Regulatory Affairs Forum

PROFESSIONAL AFFILIATIONS & CREDENTIALS

• RAPS Certification; BS Decision Science

OUTSIDE ACTIVITIES

Cycling, hiking, yoga and boating