Clinical Research Coord. Ii-Cancer Center Protocol Office

Wentworth-Douglass Hospital Boston , MA 02298

Posted 6 months ago

GENERAL SUMMARY/ OVERVIEW STATEMENT:

. The Clinical Research Associate II (CRA II) works independently under general supervision to enroll eligible patients to clinical protocols and manage all aspects of data collection and submission for multiple cancer studies.

PRINCIPAL DUTIES AND RESPONSIBILITIES:

This position represents a trained individual able to perform the following duties under general supervision by the Project/Program Manager: Verify patient eligibility via chart abstraction and clinical analysis of case data Collect and interpret data necessary for enrollment, register patients Monitor and evaluate protocol compliance Manage data collection via chart abstraction and submit data Maintain research charts for all assigned studies and enrolled patients Monitor and report adverse events as required by institutional/federal regulations Prepare submission of protocol revisions and safety reports to the IRB Prepare annual progress reports for IRB renewal of ongoing studies Organize monitoring visits as requested by sponsors and make data corrections as required by monitor Resolve data discrepancies Assess impact of new risk information on consent documents and revise appropriately

SKILLS/ABILITIES/COMPETENCIES REQUIRED:

  • Ability to work independently and as a team member High degree of computer literacy Analytical skills and ability to resolve problems Ability to interpret acceptability of data results Working knowledge of data management program

BA/BS degree required. Minimum of 1-2 years of related experience or completion of the CCPO New Staff Orientation program including completion of competency assessment

Candidates without relevant experience will be hired as CRC I


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Clinical Research Coord. Ii-Cancer Center Protocol Office

Wentworth-Douglass Hospital