Study Supervisor Position Available In Bronx, New York
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Job Description
Conduct study start up activities for all assigned clinical trials. Manage the clinical trial master files. Managing patient study calendars, facilitating patient accrual, oversight and administration of database for central record-keeping. Ensuring compliance of patients to protocol, verify patient eligibility, register patients in EPIC/Velos in accordance with Research Billing Compliance Guidelines. Perform protocol specified procedures. Schedule subjects for research tests and obtain results. Communicate results to research coordinator. Work closely with research team in the management of each patient accrued to each study. Enter subject study data into database. Maintains study documentation, study binders and completion of regulatory documentation. Prepare for site monitor visits. Prepare reports of patient enrollment for each study and review the data including performance audits. Participate in meetings with the research team to discuss new procedures that should be implemented for the management of data. Provide administrative support to the Clinical Trial Managers including creating and distributing pre-selection questionnaires, consent forms, IRB and CRC applications, BRANY/ICTR applications and FDA documentation.
Minimum Salary:
75,816
Maximum Salary:
75,816
Salary Unit:
Yearly
