Multiple Myeloma Clinical Research Associate - Cancer Center Protocol Office
Multiple Myeloma Clinical Research Associate - Cancer Center Protocol Office
Posted on :
09-04-2025
Employer Active
1 Vacancy
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Job Description
Massachusetts General Hospital is an Equal Opportunity Employer. By embracing diverse skills perspectives and ideas we choose to lead. Applications fromprotected veterans and individuals with disabilities are strongly encouraged.
CRA positions entail a high volume of data abstraction; patient contact is minimal.
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 offsite Investigator meetings
Organizes monitoring visits as requested by Sponsors and makes data corrections as required by Monitor
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 offsite Investigator meetings
Organizes monitoring visits as requested by Sponsors and makes data corrections as required by Monitor
Required Experience:
IC
Employment Type
Full-Time
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