A leading health organization in the UK is seeking a Director of Clinical Regulatory Writing to lead strategic communication for drug submissions. This role involves expert leadership to enhance clinical-regulatory documents across multiple programs. The ideal candidate will possess a Master's degree (PhD preferred), extensive experience in oncology drug development, and excellent stakeholder management skills. Join a dynamic team aiming to improve global public health through innovative solutions. Hybrid work environment with a minimum office presence of three days per week. #J-18808-Ljbffr