Clinical Scientific Review Committee Lead

About the role

The Clinical Scientific Review Committee Lead will coordinate the end‑to‑end review lifecycle for key clinical development documents across multiple therapeutic areas. Working closely with senior clinical leaders and cross‑functional teams, the role ensures high‑quality submissions, efficient governance and consistent application of review standards.

Key responsibilities

• Manage the review process for a high volume of clinical development documents from submission through approval.
• Coordinate authors, reviewers and stakeholders to ensure timely and effective reviews.
• Prepare, facilitate and document governance meetings, capturing decisions and actions.
• Provide guidance on review processes, workflows and governance requirements.
• Track documents, generate reports and manage workflow activities using collaborative document‑management systems.
• Produce operational metrics and support continuous process improvements.
• Support audit and inspection readiness through accurate documentation and governance records.
• Contribute to training, best‑practice initiatives and wider team projects.

Required profile

• Experience in clinical development, clinical operations or scientific document management.
• Knowledge of Good Clinical Practice (GCP) and clinical trial processes.
• Strong project coordination and stakeholder management abilities.
• Excellent written communication and meticulous attention to detail.

Required skills

• Good Clinical Practice (GCP)
• Document management systems