Senior Regulatory Affairs Consultant - Project Management
South Korea-Seoulonsitesenior
Posted 4 days ago · via Workday
About this role
When our values align, there's no limit to what we can achieve. At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. Required experience: Regulatory Compliance (GMP) and US NDA/EU MAA experience preferred. Minimum 7 years of experience in Pharma, Biotech, or CRO required. This role is responsible for Project Management of RA and Business Support.…
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
We compare your skills against the role requirements.
2
Level fit
This role is senior-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 based in South Korea-Seoul. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
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