Christin Lydon
Director, Regulatory Affairs, Advertising and Promotion at Vertex Pharmaceuticals
- Role
- Director, Regulatory Affairs, Advertising and Promotion at Vertex Pharmaceuticals
- Location
- Boston, MA, US
- LinkedIn followers
- 500 followers
About Christin Lydon
Regulatory Affairs leader with deep expertise in U.S. advertising and promotion strategy across rare disease, specialty, and complex therapeutic areas. I lead enterprise-critical launches and promotional governance in highly scrutinized regulatory environments, translating FDA requirements into clear, decisive strategy that enables execution while proactively managing regulatory risk.I currently provide U.S. advertising and promotion regulatory strategy for high-impact programs, setting direction for commercial, medical, patient advocacy, and corporate communications activities. I provide senior-level regulatory judgment, anticipate enforcement risk, and drive cross-functional alignment to support compliant, scalable commercialization.I also bring prior experience in Regulatory Development and labeling, supporting critical commercialization strategy from early development through launch. Combined with experience leading and mentoring high-performing regulatory professionals and strengthening governance and processes, I serve as a trusted authority on FDA advertising and promotion regulations and enforcement trends, with a focus on enterprise impact and advancing complex therapies.
Experience
Director, Regulatory Affairs, Advertising and Promotion
Jun 2022 — Present · Boston, MA, US
Education
Worcester State University
Bachelor of Science, Chemistry
2009 — 2012
Fitchburg State University
Bachelor of Science - BS, Criminal Justice
2006
Stanford University
Certificate in Medical Statistics
2020
Northeastern University
Master's of Science, Regulatory Affairs
2012 — 2014
Skills
- Fda
- Clinical Trials
- Gmp
- Pharmaceutical Industry
- Regulatory Affairs
- Oncology
- Medical Devices
- Biotechnology
- Chemistry
- Regulatory Submissions
- Sop
- Drug Development
- Clinical Research
- Life Sciences
- Ind
- Gcp
- Analytical Chemistry
- Hplc
- Regulatory Requirements
- Clinical Development
- Pharmaceutics
- U.s. Food and Drug Administration (Fda)
- Standard Operating Procedure (Sop)
- Us Labeling
- Cta
- Opdp
- Fda Opdb
- Hematology
- Advertising and Promotion
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