Regulatory Manager, Strategy - CMC RA Vaccines Development Projects
Belgium-Wavreremotemanager$59K – $98K
Posted today · via Workday
About this role
About the role Responsible for the CMC regulatory activities in the investigational, late phase development and/or early commercial lifecycle management of GSK products. About the responsibilities - Be responsible for the global CMC regulatory activities for assigned projects and responds readily to changing events and priorities - Be responsible for CMC strategy development, with managerial support, for CMC submission documents from early phase clinical submissions (IND/IMPD) through to marketing applications (NDA/BLA/MAA) and early lifecycle management activities in accordance with the applicable regulatory & scientific standards.…
Read the full description on Laboratoire GlaxoSmithKline's site →
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
For this role: r, teams
2
Level fit
This role is manager-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is remote-eligible. We factor in your stated location and time-zone overlap.
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