Senior Medical Writer, Regulatory CSR/Protocol Lead

A global biopharmaceutical solutions organization is seeking a Senior Medical Writer to lead the creation of regulatory documents, including clinical study protocols and reports. The ideal candidate will have a relevant degree and extensive experience in medical writing along with a strong understanding of regulatory standards. Responsibilities include mentoring junior writers and ensuring all writing deliverables meet quality standards. This role offers a salary between $80,600 and $145,000, depending on experience, with benefits such as healthcare and a flexible PTO policy.
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