CLINICAL RESEARCH COORD II - Oncology
CLINICAL RESEARCH COORD II - Oncology
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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.
General Summary:
As a direct report to the Clinical ResearchNurse Manager the Clinical Research Coordinator II (CRC II) works closely with the Clinical Research Associates (CRA) to screen potential patients for eligibility criteria schedule protocol required diagnostic studies schedule MD/NP health assessments and assist with data management.
The CRC works closely with the Clinical Research Nurse. These activities may require clinical skills such as phlebotomy EKG vital signs and laboratory responsibilities of blood tissue and urine procurement processing and shipping.
For daytoday responsibilities they work directly with the disease based clinical research nurse(s). The following job duties will be performed independently: Have comprehensive knowledge of all assigned protocols Develop protocol specific flow charts intake sheets and other tools as needed to ensure protocol compliance and proper data acquisition Schedule all protocol required evaluations (physical exams radiology labs etc. Coordinate patient appointments with physicians nurses and all test areas Attend Investigator meetings which establish required procedures Attend research focused disease based team meetings In cooperation with the SPL (Sample Processing Lab) coordinate obtain (e.g. draw bloods) process (e.g. spin/separate/freeze samples) and ship (e.g. utilization of specific packaging and ensuring proper handling and shipping of samples) all protocol required tissue samples Obtain vital signs EKG as indicated coordinate clinical safety laboratory specimen draws and ensure timely results are available to healthcare providers Maintain accurate patient research files and records of sample procurement Maintain study supplies and utilizes study specific supplies as required Assist primary CRA of each study with data management tasks as needed
Competency in all clinical skills (either during orientation or proof of certification on hire) is required.BA BS required Principal Duties and Responsibilities:The CRC II reports directly to the Clinical Research Nurse Manager for overall job performance.
Required Experience:
Chief
Employment Type
Full-Time
