Clinical Scientific Review Committee Lead
other jobs Cpl Life Sciences
Added before 4 Days
- England,London,City of London
- Full Time, Contract
- Salary negotiable
Job Description:
Full job descriptionClinical Scientific Review Lead
Location: Flexible UK/Hybrid London
Industry: Pharmaceutical / Clinical Development
CPL Life Sciences are collaborating with a global Pharmaceutical business based in London who are looking for an experienced clinical development professional to join their team, supporting the scientific review and governance of clinical development documents across multiple therapeutic areas.
As the Central Scientific Review Lead, you’ll 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. Working closely with senior clinical leaders and cross-functional teams, you’ll play a key role in supporting the delivery of clinical development programmes.
Key responsibilities include:
- Managing the review process for a high volume of clinical development documents from submission through to approval.
- Coordinating with authors, reviewers, and stakeholders to ensure timely and effective reviews.
- Preparing, facilitating, and documenting governance meetings, including capturing key decisions and actions.
- 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.
- Supporting audit and inspection readiness through accurate documentation and governance records.
- Contributing to training, best practice initiatives, and wider team projects.
About You:
- Experience in clinical development, clinical operations, or scientific document management.
- Knowledge of GCP and clinical trial processes.
- Strong project coordination and stakeholder management skills.
- Excellent written communication and attention to detail.
- Experience using document management or collaborative review systems is an advantage.
Please apply here if this position if of interest to you. You can also follow up with for further information.
Location: Flexible UK/Hybrid London
Industry: Pharmaceutical / Clinical Development
CPL Life Sciences are collaborating with a global Pharmaceutical business based in London who are looking for an experienced clinical development professional to join their team, supporting the scientific review and governance of clinical development documents across multiple therapeutic areas.
As the Central Scientific Review Lead, you’ll 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. Working closely with senior clinical leaders and cross-functional teams, you’ll play a key role in supporting the delivery of clinical development programmes.
Key responsibilities include:
- Managing the review process for a high volume of clinical development documents from submission through to approval.
- Coordinating with authors, reviewers, and stakeholders to ensure timely and effective reviews.
- Preparing, facilitating, and documenting governance meetings, including capturing key decisions and actions.
- 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.
- Supporting audit and inspection readiness through accurate documentation and governance records.
- Contributing to training, best practice initiatives, and wider team projects.
About You:
- Experience in clinical development, clinical operations, or scientific document management.
- Knowledge of GCP and clinical trial processes.
- Strong project coordination and stakeholder management skills.
- Excellent written communication and attention to detail.
- Experience using document management or collaborative review systems is an advantage.
Please apply here if this position if of interest to you. You can also follow up with for further information.
Job number 3897936
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Company Details:
Cpl Life Sciences
Company size: 50–99 employees
Industry: Scientific
CPL UK is a group of Specialist Talent businesses which service the Professional Services, Science, Technology, Engineering, Mathematics and Health se...