- Is subject recruitment taking longer than anticipated?
- Are the sites you are working with struggling to complete all the study specific tasks, while also providing their normal standard of care?
Having experienced clinical or non-clinical operatives on site can enable faster recruitment, improved trial experience and easier workload management. In real terms, this means:
For the sponsor and CRO:
- You have dedicated trial resources at the Investigative site(s)
- Your study benefits from faster subject identification and recruitment
- The recruitment potential for your sites is clearer
- The subject enrollment for your sites can increase
- You have a clearer view of where your Clinical Research Associates need to focus their efforts
- You have more choice in site selection, potentially opening up large new patient populations
For the site staff:
- You have dedicated study specific resources to reduce the burden of clinical trials on your team
- You have an improved subject recruitment rate
- You have additional support with high through put of subjects
- You have the potential to increase the number of clinical trials being run through your site
- You can work on trials that your internal team doesn’t have the relevant experience to support with
For the subject and their families:
- It is more likely that you can be considered for a trial
- You have more time with the site staff to complete the procedures and answer any questions you might have
