Clinical Document Review Lead

Desired Skills: clinical document,scientific review,document review,clinical trial

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
• Rate: £259.36 per day
• Location: London (hybrid)

The Role

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.

Key Responsibilities

• Manage the review lifecycle for a high volume of clinical development documents.
• 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.
• Maintain document management systems, collaborative authoring platforms and tracking tools.
• 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.

Requirements

• 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.
• Familiarity with document management systems and collaborative authoring tools.
• Excellent organisational, communication and stakeholder management skills.
• Strong scientific writing, meeting facilitation and project coordination experience.
• Ability to work effectively within a global, cross-functional environment.

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in UK***

Interested candidates should submit an updated CV.

Please click the link below to apply.