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Job description
SimulStat Inc. seeks a Sr. Medical Writer to support the development of global regulatory documentation strategy and the execution of tactics.
You will conceptualize and develop medical communications for reviewer-friendly clinical documents to support regulatory agency review, coordinating progress against global regulatory plans. The role requires a strong background in medical writing, regulatory submissions, and project management, with 6–8 years of industry experience and advanced degrees
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Worksite address
summit, NJ, 07902, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.