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Under direction of the Principal Investigator and/or designee, independently carries out studies. Responsible for screening patients for trial participation, enrolling patients, monitoring protocol implementation, completing required forms, reporting results and regulatory submission. Creates study-specific data collection and statistical and analytical reports. Responsible for managing and coordinating the clinical studies as members of the research team and will work closely with multidisciplinary teams and participate in subject research activities throughout the studies. May assist in writing articles and summarizing papers for submission.
Job Responsibility:
Responsible for daily operations of the study
Consents and enrolls patients for studies
Coordinates and prepares necessary documentation for Institutional Review Board (IRB) and external stakeholders
May prepare, monitor, and justify project budgets
Serves as liaison between local study sites and Clinical Coordinating Center
Creates tracking systems
Create and prepare data collection statistical reports and analytical summaries
Assists PIs in preparing new applications for research funding and in developing, implementing, and managing ancillary study grants
Requirements:
A Bachelor's Degree is required, Master's Degree preferred
A minimum of 2 years of relevant experience is required
Experience with RedCap and EPIC is preferred
Nice to have:
Master's Degree
Experience with RedCap and EPIC
What we offer:
flexible schedules
affordable health, vision and dental insurance
child care and student loan subsidies
generous levels of time off
403(b) Retirement Savings plan
Pension
Tuition and certain License and Certification Reimbursement