Senior Regulatory Medical Writer & Team Lead

A clinical-stage oncology company in Redwood City is seeking a Clinical Regulatory Writer to lead the preparation of high-quality clinical research documents for drug development. The ideal candidate will have over 8 years of experience and an advanced degree in life sciences or similar fields. Responsibilities include managing and drafting regulatory documents, mentoring junior writers, and ensuring deliverables meet quality standards. This position offers a dynamic work environment focused on innovative cancer therapies. #J-18808-Ljbffr