Cpl Life Sciences
Clinical Scientific Committee Review
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Clinical Scientific Committee Review
Clinical Scientific Committee Review
📍 Location
Flexible UK/Hybrid London
🏫 Industry
Pharmaceutical / Clinical Development
⏳ Duration
12 month contract
CPL Life Sciences are collaborating with a global Pharmaceutical business based in London seeking an experienced clinical development professional.
The role of Central Scientific Review Lead:
This position requires you to coordinate the end-to-end review lifecycle for key clinical development documents. Ensuring high-quality submissions, efficient governance processes and consistent application of review standards, you’ll work closely with senior clinical leaders and cross-functional teams.
Key Responsibilities
- Efficient management of the review process for high volumes of clinical development documents from submission through to approval.
- Coordination with authors, reviewers, and stakeholders to ensure timely and effective reviews.
- Preparation, facilitation and documentation of governance meetings. This includes capturing key decisions, actions, and progress updates.
- Providing guidance on review processes, workflows, and governance requirements.
- Managing document tracking, reporting and workflow activities using collaborative document management systems.
- Producing operational metrics and supporting continuous process improvements.
- Ensuring audit and inspection readiness through accurate documentation and governance records.
- Contribution to training, best practice initiatives, and wider team projects.
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About You: Requirements & Qualifications
- Proven experience in clinical development, clinical operations, or scientific document management.
- Strong knowledge of GCP (Good Clinical Practice) and clinical trial processes.
- Excellent project coordination, stakeholder management skills.
- Outstanding written communication and attention to detail.
- Experience using document management or collaborative review systems preferred.
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How to Apply
If this opportunity aligns with your expertise, apply [here]. For further details, follow up with: sarah.phillips@cpl.com.
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