Senior Medical Writer, Oncology Regs (Remote, US)

A clinical-stage biopharma company is seeking an experienced Senior Medical Writer to lead the creation of high-quality clinical and regulatory documents for oncology programs. This remote position requires a minimum of 7 years of medical writing experience, including authorship of BLA clinical modules and CSRs. The role demands strong collaboration across functions and a thorough understanding of ICH, FDA, and EMA guidelines. Candidates should be able to translate complex results into clear narratives and manage submission readiness efficiently. This opportunity offers a competitive salary alongside a supportive and mission-driven environment. #J-18808-Ljbffr