What Makes a Great CRA-Site Partnership?
In this newly published episode of Seamless Insights: The Podcast, Hamish Baird, President of Remington Davis, sits down with Medpace Sr. CRA Manager Meera Gosalia to discuss what makes clinical research associates (CRAs) effective partners at the site level. Drawing on nearly three decades of industry experience, Hamish shares real-world perspectives from the research site side – including how strong communication, protocol expertise, and consistent collaboration can help sites navigate increasingly complex clinical trials.
From practical examples of reducing screen failure rates to improving data entry workflows and recruitment strategies, the conversation highlights how experienced CRAs can help sites work more efficiently while maintaining high standards for data quality and patient care.
Supporting Sites to Deliver High-Quality Trials
CRAs play a critical role in ensuring studies run smoothly, from maintaining regulatory compliance to supporting sites with practical solutions that improve study conduct. By combining deep protocol knowledge with strong communication and site awareness, Medpace CRAs work as true partners to research teams throughout the trial lifecycle.
Working closely with clinical trial managers and global project teams, our CRAs help sites address operational challenges, share best practices across studies, and maintain the consistency needed to deliver reliable, high-quality clinical data.