Site Data Coordinator Ii
Acorn Research, Llc
Selected Achievements: Selected to support the activities of clinical trials involving various oncology diseases.Duties include completing case report forms and resolving discrepancies in supporting documentation and accepting additional duties as assigned. Trials currently under way. Familiar working with EDC systems (Medidata Rave, Inform, Timaeus,and INC Research) as well as various MOSAIQ, CISCO, and Citrix EMS systems from clinics throughout the US. Review source documentation and… Show more Selected Achievements: Selected to support the activities of clinical trials involving various oncology diseases.Duties include completing case report forms and resolving discrepancies in supporting documentation and accepting additional duties as assigned. Trials currently under way. Familiar working with EDC systems (Medidata Rave, Inform, Timaeus,and INC Research) as well as various MOSAIQ, CISCO, and Citrix EMS systems from clinics throughout the US. Review source documentation and responds promptly to sponsor inquires. Generate site queries for missing information. Ensure Serious Adverse Event (SAE) reporting according to project specifications. Provides regular clinical status information to team members and project management. Communicate with site personnel to resolve both internal and external queries. Review and evaluate the quality of CRF completion prior to monitor visits. Meet with monitor during the visit to complete CRF corrections. Maintain subject screening/enrollment logs. Prepare for any study audits that might be conducted. Assist Director of Data services with data base maintenance. Coordinate and participate in internal and external meetings as needed. Participate in departmental meetings with Project management, Regulatory affairs and ACORN sites. Interface with multiple functional departments including Data Management, Project Management, Regulatory Affairs, Sponsors and CROs Show less