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. 

In this all-new webinar, industry experts from various disciplines will discuss the research from the perspectives of the patient, site staff, sponsor, and technology provider.

Access this recording to uncover:

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