Neuro Oncology Clinical Research Coord. II-cancer Center Protocol Office
NEURO ONCOLOGY CLINICAL RESEARCH COORD. II-CANCER CENTER PROTOCOL OFFICE
CRA positions entail a high volume of data abstraction; no patient contact. Manages the following for multiple studies:
' Verifies patient eligibility via chart abstraction and clinical analysis of case data
' Collects and interprets data necessary for enrollment; registers patients
' Instructs Clinical Research Coordinators in protocol evaluations/samples needed
' Monitors and evaluates protocol compliance
' Manages data collection via chart abstraction and submits data in timely fashion
' Monitors and reports adverse events as required by institutional/federal regulations
' Coordinates and procures investigational drug supplies
' Resolves data discrepancies as requested by Sponsors
' Coordinates and processes tissue samples as required by protocol
' Prepares submission of protocol revisions and safety reports to the IRB
' Prepares annual progress reports for IRB renewal of ongoing studies
' Organizes and attends on- and off-site Investigator meetings
' Organizes monitoring visits as requested by Sponsors and makes data corrections as required by Monitor
The focus of this position is Neuro Oncology Clinical Trials. As a direct report to the Clinical Research Program Manager the entry level Clinical Research Associate works closely with Investigators to recruit eligible patients to clinical protocols and manages all aspects of data collection and submission for multiple cancer trials.
BA/BS degree required and minimum of 1-2 years of related experience OR completion of the CCPO New Staff Orientation program including completion of competency assessment.
Candidates with no relevant experience will be hired as Clinical Research Coordinator I.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
CRA positions entail a high volume of data abstraction; no patient contact. Manages the following for multiple studies:
' Verifies patient eligibility via chart abstraction and clinical analysis of case data
' Collects and interprets data necessary for enrollment; registers patients
' Instructs Clinical Research Coordinators in protocol evaluations/samples needed
' Monitors and evaluates protocol compliance
' Manages data collection via chart abstraction and submits data in timely fashion
' Monitors and reports adverse events as required by institutional/federal regulations
' Coordinates and procures investigational drug supplies
' Resolves data discrepancies as requested by Sponsors
' Coordinates and processes tissue samples as required by protocol
' Prepares submission of protocol revisions and safety reports to the IRB
' Prepares annual progress reports for IRB renewal of ongoing studies
' Organizes and attends on- and off-site Investigator meetings
' Organizes monitoring visits as requested by Sponsors and makes data corrections as required by Monitor
The focus of this position is Neuro Oncology Clinical Trials. As a direct report to the Clinical Research Program Manager the entry level Clinical Research Associate works closely with Investigators to recruit eligible patients to clinical protocols and manages all aspects of data collection and submission for multiple cancer trials.
BA/BS degree required and minimum of 1-2 years of related experience OR completion of the CCPO New Staff Orientation program including completion of competency assessment.
Candidates with no relevant experience will be hired as Clinical Research Coordinator I.
. Apply now!Estimated Salary: $20 to $28 per hour based on qualifications.
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