Associate Director, R&I Clinical Regulatory Writing (CReW)
US - Gaithersburg - MDonsitedirector
Posted today · via Workday
About this role
We are now recruiting a n Associate Director , R&I Clinical Regulatory Writing ( CReW ) . A s part of a clinical delivery or submission team, the Associate Director provide s strategic communications leadership to projects, establish es communication standards and best practice, and continuously advocate s for quality and efficiency. The Associate Director also a uthor s strategic clinical-regulatory documents and provid es critical review to achieve high-quality standards, utilizing best practices for document and accelerated submission delivery . What You will Do The Associate Director, CReW , is expected to: Independently manage clinical regulatory writing activities across a portfolio of work.…
Read the full description on 4314 Astra Zeneca Pharmaceuticals LP'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
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2
Level fit
This role is director-level. We check your trajectory against it.
3
Domain experience
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4
Recency
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5
Location fit
This role is based in US - Gaithersburg - MD. We weight your proximity and willingness to relocate.
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