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Medical Writing Director
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About Richmond Pharmacology
Richmond Pharmacology is a leading Contract Research Organisation (CRO) specialising in early-phase clinical trials for pharmaceutical and biotechnology sponsors. With a commitment to excellence and innovation, we strive to advance medical research and contribute to the development of life-changing therapies.
Job OverviewWe are seeking an experienced and accomplished Head of Medical Writing and Regulatory Submissions to lead and develop our medical writing and regulatory teams. In this senior role, you will play a pivotal part in overseeing the preparation of high-quality regulatory submissions and medical writing deliverables, ensuring clarity, accuracy and compliance with regulatory standards.
This role involves managing the entire medical writing and regulatory submissions process, liaising directly with sponsors, regulatory authorities and ethics committees. You will be responsible for high-level Quality Control (QC) across all documents, ensuring consistency and regulatory compliance. Additionally, this role involves mentoring and supervising less experienced team members and overseeing the continuous updating of Standard Operating Procedures (SOPs) and document templates to align with the latest regulatory guidelines.