Oncology trials are uniquely difficult to plan and run, due to the complexity of endpoints and assessment criteria, and the frequently changing requirements. And yet, study managers are still under pressure to meet timeline goals that are heavily dependent on patient recruitment and retention, while managing study design and protocol amendments. 

Watch the webinar to hear about related topics that include:

The importance of easy-to-use technology to improve patient retention

New ways to accelerate start-up and protocol amendment implementation

Why patient-centricity matters to improved data collection

How to manage complex study designs, and more