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 strategic labelling staff
GSK is seeking a Director for Labelling Strategy & Development, focusing on early lifecycle labelling in therapeutic areas such as Oncology and Vaccines. The role demands extensive regulatory experience and leadership capabilities, with a hybrid work model requiring on-site collaboration 2-3 days a week
Job Summary
The role is accountable for directing global delivery and early lifecycle labelling development for assigned therapeutic areas including Oncology and Vaccines.
Candidates must possess at least five years of regulatory affairs experience with line leadership capabilities within the pharmaceutical industry.
This hybrid position requires regular on-site collaboration, typically 2 to 3 days per week, to ensure cohesive end-to-end labelling approaches.
Matching Summary
Match Score: 85
GSK is seeking a Director for Labelling Strategy & Development, focusing on early lifecycle labelling in therapeutic areas such as Oncology and Vaccines. The role demands extensive regulatory experience and leadership capabilities, with a hybrid work model requiring on-site collaboration 2-3 days a week.
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 strategic labelling staff
Bachelor's degree in life sciences or pharmacy
Experience with FDA and EMA regulations
Nice-to-have
Advanced degree in scientific discipline
Direct interaction with regulatory reviewers
Patient-focused plain-language content development
Mentoring and building team capability
Collaborative and curious problem solver
Key Requirements
Bachelor's degree in life sciences, pharmacy, or medicine