Clinical Research Associates (CRAs) are the foundation for successful delivery of your trial. Cmed’s seasoned CRAs are dedicated to the integrity of your study data and patient safety, ensuring quality through both onsite and remote monitoring. Site investigators and teams consistently tells us that they value the partnerships our CRAs establish and the demonstrated level of skill and commitment brought to their sites.
> Have the experience and skills to deliver trials within a wide
range of therapeutic areas, including indications that are rare
and highly complex to treat.
> Understand the standards of care associated with each trial and
importance of patient safety; site management is a holistic
approach to ensuring regulatory and study compliance is maintained.
> Have a turnover rate well below industry average, a testament to
both the culture at Cmed and the great working relationship they have
with our sites and customers.