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.