Senior Medical Writer - Regulatory CSR/Protocol (Late Phase)

A leading biopharmaceutical solutions organization is seeking a Senior Medical Writer to manage regulatory documents, coordinate writing activities, and mentor junior writers. Responsibilities include completing clinical study protocols and reports while ensuring compliance with regulatory standards. Ideal candidates will have at least 3 years of medical writing experience and a strong understanding of ICH E3 guidelines. This role offers a competitive salary range from $80,600 to $145,000, alongside a range of benefits.
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