How To Partner With Your CRA For Best Trial Outcomes

In a conversation about the collaboration between clinical research sites and CROs, Jen Stacy, Director of Clinical Operations at Novotech, shares insights on how to build stronger, more effective partnerships. Drawing on her background as a cardiac critical care nurse, Stacy emphasizes the shared goal of protecting patients and ensuring the success of clinical trials, particularly for small biotech companies.

The discussion addresses common challenges like site payments and protocol deviations, highlighting that an open and proactive relationship with a Clinical Research Associate (CRA) is crucial. Instead of just a monitor, a CRA can serve as a site's advocate, helping to streamline processes, find creative solutions to problems, and address potential issues before they become major hurdles. Stacy discussed how transparent and early communication is the cornerstone of a successful trial, allowing teams to set realistic expectations and work together to achieve data quality and compliance. Ultimately, this collaborative mindset is essential for navigating the complexities of clinical research and ensuring a smooth journey from study start-up to regulatory submission.