Senior Medical Writer & Regulatory Lead

A data-focused CRO is seeking an experienced Medical Writer to evaluate medical literature and produce clinical development documents. The ideal candidate will have 3-5 years of regulatory writing or clinical medical writing experience, and be proficient in MS Office tools. Strong writing skills, the ability to handle complex clinical information, and excellent organizational abilities are essential. This role involves direct client interactions and mentoring of junior writers, contributing to the success of clinical projects in the pharmaceutical industry. #J-18808-Ljbffr