Lead Medical Writer & Project Lead – Regulatory Expert

IQVIA in Reading is seeking a Lead Medical Writer to oversee various writing projects while ensuring compliance with established SOPs and timelines. The ideal candidate will possess at least 7 years of regulatory writing experience and have a background in life sciences with relevant qualifications. The role demands excellent communication skills and the ability to negotiate with customers effectively. Join IQVIA’s dynamic team and contribute to the advancement of drug development through high-quality medical writing.#J-18808-Ljbffr…