PE Global is currently recruiting for a Clinical Document Review Lead on behalf of a leading global pharmaceutical company. This is an excellent opportunity to join a global Clinical Development team, supporting the review, coordination and governance of key clinical documents across multiple therapeutic areas. Duration: 12-month contract Location: London (hybrid) As the Clinical Document Review Lead, you will oversee the end-to-end review process for critical clinical development documents, including concept sheets, study protocols and clinical development plans. Acting as the central coordinator for the scientific review process, you will work closely with senior clinical leaders and cross-functional teams to ensure documents are reviewed efficiently, meetings are well managed and governance processes are followed. This is a highly collaborative role that combines project management, stakeholder engagement and clinical document oversight to support the delivery of high-quality clinical programmes. Coordinate document submissions, review timelines and stakeholder communications. Prepare and facilitate scientific review meetings, ensuring accurate agendas, documentation and meeting minutes. Provide guidance on document review processes, workflows and governance requirements. Produce key performance metrics and support reporting activities. Contribute to process improvements, training initiatives and best practice sharing. Support audit and inspection readiness through robust documentation and process compliance. Bachelor's degree in Life Sciences or a related scientific discipline (advanced degree preferred). Minimum 5 years' experience within the pharmaceutical industry. Strong knowledge of clinical drug development, clinical trial design, GCP and regulatory requirements. Experience managing clinical documents and review processes within Clinical Development. Strong scientific writing, meeting facilitation and project coordination experience.
