Precision’s global footprint enables excellence in the implementation of clinical trials on a global scale and supports the challenges faced by sponsors through all facets of the trial. Innovators of novel oncology compounds are often confronted with the following challenges when executing their global clinical trials:
• Identifying and accessing the best global sites
• Understanding their need for validated assays for their biomarkers
• Expediting study start-up
• Regulatory and Ethics filings
• Efficiently handling samples globally and in real-time
• Fulfilling the need for high-quality data and results
• Ensuring robust trial execution to support regulatory submissions
Precision Oncology’s expert team of clinical research professionals is there to support you through each step of your trial—wherever the research takes place.
Our scientific teams can help define biomarker identification and patient stratification approaches, and implement these needs globally - from PBMC isolations to protein and gene expression to immune response assays.
Rapid Study Start-up
The sites in our Global Oncology Site Network strive for and are committed to a 90-day start-up. Our global operational platform provides a robust foundation for bringing on sites for rapid starts. Regulatory experts on staff ensure high quality, rapid submissions and ethics review.
Quality Clinical Operations, Data and Results
We provide centralized and regional project management services. We have hundreds of well-retained and experienced clinical monitors and project managers. Strong focus and rigorous processes help ensure that clinical and biomarker data is of the highest quality.
Clinical operations experts provide in-country expertise to support regulatory and ethics committee filings. Full and expert analytics services are available globally. We specialize in trial execution with documented quality, to fully support regulatory submissions.
Global Lab Services
Our global laboratory network ensures high-quality samples are prepared, managed and available when needed for validated assays. We can collect and process samples taken throughout the world, usually in 24 hours and in no more than 48.