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A leading health research organization in Warsaw is seeking a Principal Medical Writer to lead the production of regulatory submission documents. The ideal candidate will have 3-5 years of experience in medical writing within the biopharmaceutical industry and a strong understanding of FDA and ICH regulations. Responsibilities include overseeing the completion of various complex documents and ensuring compliance with regulatory standards. This role offers a competitive salary and benefits including health, 401k match, and flexible paid time off.
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