OUTSOURCING


A clinical research data collection partner for the ‘new normal’


Rob Ramirez, chief client officer at Schlesinger Clinical Research, answers critical questions that clinical researchers should ask when outsourcing clinical data collection in these challenging times.


How suited are your sites to safely manage in-person studies during a pandemic? Rob Ramirez: No matter how well a site has performed before the Covid-19 pandemic, undertaking responsible in-person clinical research includes confirming that new and effective protocols are in place to maximise the safety of all on-site stakeholders. Schlesinger sites are high-specification


private data collection and testing spaces. We have been successfully conducting in-person research under new the protocols to ensure our sites are safe. Protocols include screeners around symptoms, electrostatic sanitising, temperature


taking, acrylic screen guards, physical distancing and respiratory hygiene. Clients and clinical teams on-site can view testing separately in one-way mirror viewing rooms and lounges. Remote stakeholders are able to stream the sessions or download HD recordings within an hour of completion. As every project is unique, we customise our flexible sites to clients’ clinical study specifications and precaution preferences.


How do you ensure consistency of study protocols across multiple sites? Consistency of site environment, approach and protocols are some of the key challenges of


20 | Outsourcing in Clinical Trials Handbook


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