Job Description:

Position Overview:In this role you will ensure IRB approved protocols are implemented and followed; execute theinformed consent process and monitor patient status and safety; collect and organize researchdata; schedule and conduct study-specific training and site in-services to study related staff onnew or amended protocols, and educate patients and their families about treatments andpossible side effects. The Clinical Research Coordinator must also be able to perform clinicaltasks.Responsibilities:â— Site preparation.â— Obtaining informed consent, patient screening and recruitment.â— Patient enrollment, and conducting study visits.â— Maintaining and dispensing study product and supplies.â— Completing and ensuring the quality of case report forms.â— Maintaining source documentsâ— Ensuring site quality.â— Maintain a thorough and meticulous working knowledge of protocol schemas andâ— requirements.â— Collaborate with physicians to maintain strict protocol adherence and serve as aâ— resource for members of staff.â— Writes patient information sheet for clinical studies for submission to IRB, as well asâ— complete the necessary documents for IRB admission in a timely fashion.â— Participate in the development and implementation of patient educational materials.â— Writes patient information sheet (ICF) for clinical studies for admission to IRB, as well asâ— complete the necessary documents for IRB submission in a timely fashion.â— Review research and administrative documents to determine action items, prioritizingâ— and tracking action items.â— Responsible for completion, submission and tracking of regulatory documents to theâ— IRB.â— Maintain and update research fund accounting files, research billing, budgets andâ— transfer of funds.â— Respond to correspondence, data and informational requests.â— Analysis of statistical, resource, performance and budget data and generation of reports.