Children's Hospital Colorado Clinical Research Coordinator - 59639 in Aurora, Colorado

Why Work at Children's....Children's Hospital Colorado has defined and delivered pediatric healthcareexcellence for more than 100 years. Founded in 1908, Children's Coloradois a leading pediatric network entirely devoted to the health and well beingof children. Continually recognized as one of the nation's outstandinghospitals by U.S. News & World Report, Children's Colorado is known bothfor its nationally and internationally recognized medical, research andeducation programs as well as the full spectrum of everyday care for kidsthroughout Colorado and surrounding states. With more than 1,000 healthcareprofessionals representing the full spectrum of pediatric specialties,Children's Colorado Network of Care includes its main campus, 16Children's Care Centers and more than 400 outreach clinics.A career at Children's Colorado will challenge you, inspire you, andmotivate you to make a difference in the life of a child.Additional InformationDepartment: RI-CCROHours per week: 40, eligible for benefitsShift: Full-Time Monday through FridayJob OverviewThe Clinical Research Coordinator is responsible for participating in theday-to-day operations of assigned clinical research programs and/or studiesconducted by Principal Investigators (PIs) at the University of ColoradoAnschutz Medical Campus. Performs a variety of administrative and operationalduties involved in the collection, compilation, documentation and reviewof clinical research data. Supports the achievement of research programand/or study objectives. Works under close supervision.ResponsibilitiesPopulation Specific CareNeonate -Infancy - >30 days to 1yrToddlers - >1yr to 3yrsPre-Schoolers - >3yrs to 5yrsSchool age - >5yrs to 13yrsAdolescent - >13yrs to 18yrsAdult - >18yrs to 65yrsEssential FunctionsAn employee in this position may be called upon to do any or all of thefollowing essential functions. These examples do not include all of thefunctions which the employee may be expected to perform.Submits studies for review and approval and provides status updates throughoutthe startup process. Assists regulatory team with Institutional Review Board(IRB) preparation and submission.Screens, schedules, consents participants in a variety of clinicalresearch programs and/or studies. Explains the difference between clinicalactivities and research activities, risk and benefits of study participationto participants.Assists with developing or develops protocol-specific systems and documentsincluding process flows, training manuals, Standard Operating Procedures(SOPs) and Case Report Forms (CRFs). Maintains subject leveldocumentation and prepares documents, equipment and/or supplies.Conducts and documents visits and testing/interviews according to allregulatory and organizational protocols. Collects, prepares, processes,ships and maintains inventory of research specimens.Collects information to determine feasibility, recruitment and retentionstrategies. Employs strategies to maintain participant recruitment andretention rates and assists participants with individual needs.Collects, prepares and/or processes Adverse Event (AE) information perprotocol and provides input for AE reports. May complete and submit AEreports, according to institution and sponsor-specific reporting requirements.Provides input for and assists with developing IRB related documents.Maintains or collaborates to maintain appropriate documentation.Assists with identifying issues related to operational efficiency and sharesresults with management.Maintains compliance with institutional requirements and policies. Developsand maintains a familiarity with the ethical conduct of research andsafeguards needed when conducting clinical research. May assist with thedesign of safeguards to ensure ethical conduct and to protect vulnerablepopulations.Participates in sponsor-required training. Obtains information for orcoordinates operational plans for multiple research programs and/or studies.Prepares for and participates in team m