Clinical site coordinators outsourcing

Smooth Drug Development offer outsourcing of clinical site coordinators. Coordinators can work on both full-time as well as part-time basis.
Our coordinators can be assigned to sites to assist with routine non-medical work:
  • Telephone contacts with patients to offer participation in a study
  • Calling patients to scheduled visits
  • Controlling patients’ visits to the site according to the flow chart in the Study Protocol
  • Preparing questionnaires and laboratory kits for patients` visits
  • Working with logs, documents collection, investigator file maintenance
  • Completing Case Report Forms and answering queries
  • Interacting with a patient on non-medical matters
  • Maintaining documentation with Ethics Committee
  • Working with CRAs
The benefits for site include:
  • Availability for calls from patients, CRAs and other members of the study team
  • Optimization of doctors’ workload – possibility to enroll more patients into the study
  • Better Protocol compliance and data quality
The benefits for Sponsor include:
  • Faster site initiation and start-up
  • Internal control of study team work
  • Fewer mistakes – less work for the CRA
  • Fewer ethical violations during work with patients
  • Adherence to study study enrollment timelines.
Smooth Drug Development offers service for coordinator outsourcing since 2008.