Senior Medical Writer - Regulatory Doc Lead (Hybrid)

A biotechnology company is looking for a Senior Medical Writer to draft and manage clinical study documents and oversee project timelines. This hybrid role involves collaborating with cross-functional teams to ensure regulatory compliance and high-quality documentation. The successful candidate will have a Bachelor's degree and experience in medical writing within the pharmaceutical industry. Proficiency in Microsoft Word and regulatory knowledge are essential. Join us to make a significant impact on advancing vital therapies.