Systimmune is hiring: Medical Writer — Clinical Protocols & Regulatory Docs in P

A leading biopharmaceutical company located in New Jersey is seeking a Medical Writer to manage clinical documentation projects, including protocols and reports. The ideal candidate will hold a Master’s degree or PhD in a life sciences discipline and possess experience in the pharmaceutical industry. Responsibilities include writing and editing clinical documentation, participating in clinical trial teams, and ensuring compliance with regulatory guidelines. Competitive compensation is offered with a comprehensive benefits package. #J-18808-Ljbffr