Director, Labelling Strategy & Development, Therapeutic Area Lead
GSK
Not specified; not specified; comprehensive benefi...
Hybrid (2-3 days on-site per week)
5+ years regulatory affairs experience
3+ years global labelling development
Line management of labelling teams
GSK is seeking a Director for Labelling Strategy & Development within their Therapeutic Area Lead, responsible for overseeing global labelling processes for early lifecycle products. The ideal candidate will have extensive regulatory affairs experience, particularly in labelling for the pharmaceutical or biotech industry, and a passion for improving patient outcomes
Job Summary
The role is accountable for directing global delivery and early lifecycle labelling development for assigned therapeutic areas from Phase 2 to early lifecycle.
Candidates must possess at least five years of regulatory affairs or labelling experience with proven line and matrix leadership capabilities.
GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing while uniting science and technology.
Matching Summary
Match Score: 85
GSK is seeking a Director for Labelling Strategy & Development within their Therapeutic Area Lead, responsible for overseeing global labelling processes for early lifecycle products. The ideal candidate will have extensive regulatory affairs experience, particularly in labelling for the pharmaceutical or biotech industry, and a passion for improving patient outcomes.
Salary
Not specified; Not specified; Comprehensive benefits program offered
Skills & Requirements
Must-have
5+ years regulatory affairs experience
3+ years global labelling development
Line management of labelling teams
Bachelor's degree in life sciences
Knowledge of FDA/EMA regulations
Nice-to-have
Experience with plain-language content
Patient-focused labeling strategy
Mentoring and team building skills
Collaborative and curious mindset
Experience with industry groups like DIA
Key Requirements
Bachelor's degree in life sciences, pharmacy, medicine, or related field
At least 5 years of regulatory affairs or labelling experience
3+ years leading global labelling development or submissions
US work authorization required (implied by US benefits reference)