A clinical-stage biopharmaceutical firm in the United Kingdom is seeking a Director, Regulatory Affairs CMC. This leadership role involves developing global CMC regulatory strategies for innovative therapies aimed at cancer treatment. The successful candidate will leverage a minimum of 10 years of experience in Regulatory Affairs, involving detailed knowledge of large molecule biologics and FDA/EU regulations. They will work closely with cross-functional teams to ensure timely regulatory submissions and compliance with global requirements.#J-18808-Ljbffr…
