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Late Phase Solutions

The implementation of a clinical trial is complex and relies upon careful planning and coordination matched with robust data-driven execution. This is especially so in large, Phase II trials, which require additional layers of complexity, and a team which is experienced at delivering late phase solutions.

With the goal of demonstrating safety and effectiveness of a therapy we expect the sponsor to insist that the clinical trial implementation team executes a trial with efficiency, precision and expertise.

Delivering Quality

Cytel’s late phase clinical study implementation teams consist of specialists in Data Management, Biostatistics, Statistical Programming, Medical Writing and other key functionalities, led by an experienced team of project managers. 

Decades of management experience ensure that standard operating procedures reflect the needs of a clinical trial, while sharp industry insights shape tactical strategy. This positions teams to be responsive to unexpected challenges and transform them into opportunities. 

Whether your clinical trial design is complex and innovative, or follows the principles of traditional trial design, we deliver the quality that your clinical data deserves.

If you would like to learn more about Cytel’s expertise in late stage solutions, one of our representatives would be happy to speak to you. Just get in touch.



Clinical development productivity for high-efficiency, high-impact clinical trials.



Accomplished teams possessing advanced qualifications and accomplished managers with decades of experience in full-service, biometrics and specialized solutions. 



The triumvirate of subject-matter expertise, operational know-how and industry experience delivering quality, on time and on budget.

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