Hybrid Medical Writing Associate: Regulatory & Editorial

A clinical-stage biotechnology company is seeking a Medical Writing Associate to conduct and coordinate medical document editing and reviews in compliance with regulatory requirements. This role emphasizes quality assurance and collaboration with teams to produce high-quality clinical documents. Ideal candidates will have a background in regulatory affairs or medical writing with strong attention to detail and communication skills. This position offers a hybrid work model and a competitive salary range of $85,000 – $130,000 with bonus eligibility. #J-18808-Ljbffr