At a Glance
- Tasks: Lead the review process for clinical development documents and ensure high-quality submissions.
- Company: Global pharmaceutical company with a focus on innovation and collaboration.
- Benefits: Flexible working, competitive salary, and opportunities for professional growth.
- Other info: Join a dynamic team and contribute to exciting clinical programmes.
- Why this job: Make a real impact in clinical development while working with top professionals in the field.
- Qualifications: Experience in clinical development and strong project coordination skills required.
The predicted salary is between 55000 - 65000 £ per year.
Location: Flexible UK/Hybrid London
Industry: Pharmaceutical / Clinical Development
Contract length: 12 month contract
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 is of interest to you. You can also follow up with sarah.phillips@cpl.com for further information.
Clinical Scientific Committee Review in City of London employer: Cpl Life Sciences
Join a leading global Pharmaceutical company based in London, where you will be part of a dynamic and collaborative work culture that values innovation and excellence in clinical development. With flexible working options and a commitment to employee growth, this role offers the opportunity to engage with senior clinical leaders and contribute to impactful projects across multiple therapeutic areas. Enjoy a supportive environment that prioritises continuous improvement and professional development, making it an ideal place for those seeking meaningful and rewarding employment.
