The Pharmaceutical Leader needed extra hands dedicated to supporting its trials and data collection activities at
clinical sites already over‐burdened by heavy and active patient enrollment. Realizing the need for trained
talent, the Pharmaceutical Leader asked RxRS to staff its clinical trials with seasoned CRCs who could start work
immediately and remain committed for a 3 year period. As the study design included indication‐specific
technical data criteria, the CRCs needed to have prior significant experience in the targeted marketing
indication. CRCs were placed ‘on assignment’ at clinical trial offices, sites and university hospitals throughout the
Midwest and East Coast. Their duties included scheduling patients, data entry, documentation, and handling
patient and sponsor company queries in dedicated support to the trial.
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