Clinical Regulatory Medical Writer - Protocols & Reports

A leading clinical-stage biopharmaceutical company in Princeton, NJ, is seeking a Medical Writer to manage clinical documentation projects. Responsibilities include writing and editing clinical study protocols, regulatory documents, and collaborating with clinical trial teams to ensure high-quality submissions. Candidates should have a Master's degree or relevant experience in the pharmaceutical industry, with excellent writing and communication skills. Join a dynamic environment focused on innovative cancer treatments. Competitive salary range of $80,000 - $130,000 per year based on qualifications. #J-18808-Ljbffr