Senior Clinical Medical Writer — Lead Regulatory Documentation

A leading biotechnology firm in the United Kingdom is seeking a Principal Clinical Medical Writer to oversee medical writing staff and manage documentation for clinical development programs. The ideal candidate will have at least 8 years of experience in medical writing within the pharmaceutical industry and possess strong project management and communication skills. This role offers the opportunity to work on leading-edge treatments for genetic diseases in a collaborative environment.
#J-18808-Ljbffr