Associate Director, R&I Clinical Regulatory Writing (CReW)
astrazeneca · US - Gaithersburg - MD · $137k–$205k
- Posted
- 13 days ago
- Last confirmed live
- 4 days ago
- Published range
- $137k–$205k
What this role involves
The Associate Director, R&I Clinical Regulatory Writing (CReW) leads clinical regulatory writing activities, authors strategic documents, and drives submission communication strategy. The role requires at least 5 years of medical/regulatory writing experience in pharma/biotech or CRO, with a bachelor's degree minimum. The position offers a base pay range of $136,784.80 to $205,177.20 USD annually.
Skills this posting asks for
- clinical regulatory writing
- medical writing
- regulatory writing
- submission authoring
- drug development
- communication strategy
- matrix team collaboration
- english
Requirements
- 5 years of experience
- Level: director
Apply without filling the form
Approve this role and the application is completed for you, including a résumé tailored to it. You get a confirmation when it lands, and a credit is only spent when a submission is confirmed.
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