www.prorelixresearch.com e-Consent - Train And Communicate
Once site selection is complete and site initiation begins, eConsent should be included in all team communication and training. To ensure adequate apprenticeship, leaders should implement modules, guides and videos that prepare staff to oversee processes and best practices. www.prorelixresearch.com
A robust site adoption escalation pathway will quickly reveal any unidentified challenges that arise throughout site selection and study conduct.
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In addition, Sponsor should be ready to discuss frequently asked questions, including a checklist of items to be covered during the site initiation visit.
One way to ensure success is by providing organizers with a comprehensive list of consent-related tasks to be included in the clinical operation strategy and site monitoring plans
Build a Monitor Advocacy Program
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Once a site has been successfully activated, it is important to continue to engage with staff regarding their use of eConsent so that the efficiencies of the system in consenting, reconsenting and remote monitoring are realized.
CRAs are on the “front line” with sites and usually are the first to detect if a site requires extra support. .
The evolution to digitally enabled clinical trials is well underway, which means upfront planning and training go a long way to improving patient engagement, protocol adherence, and patient retention rates.
A Giant Leap Forward For Clinical Trials
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The time is now for trial sponsors and research sites to fully embrace eConsent platforms as the standard for optimal patient experience.
These steps help more of our fellow clinical research professionals in the industry gain the greatest value of featurerich eConsent platforms and deliver better care for the patients we all tirelessly work to support each day.
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ProRelix Research is here for the timely execution of your projects! www.prorelixresearch.com