Each clinic is responsible for achieving the monthly recruitment targets as established during the site pre-qualification. Clinics will use a variety of techniques to identify potential study subjects including:
Direct or Indirect mailing campaigns to prospective study subjects
Running queries on local subject databases
Screening campaigns through local health care providers
Advertisement (i.e. newspaper, radio, television, etc.) where applicable
Local outreach to General Practitioners (GP), Hospitals, and / or Specialists
Participation in community outreach programs that provide general clinical study information On an ongoing basis, the CCBR CSO primary contact will summarize all recruitment activities for Sponsor.
Working with CCBR speeds up and drives efficiencies in clinical trials by offering greater numbers of patients across fewer sites
A Global Footprint covering 16 dedicated Clinical Research Centers in high density population areas
Uniform SOPs enable the tightest possible adherence to study protocols and consistency across all CCBR sites
Real-Time tacking of subject enrolment and trial progress ensures sponsors have the most up to date information, all of the time
Centralised, standardised billing affords better visibility into trial costs for sponsors
