About The JobProvide administrative and regulatory assistance to the Regulatory Affairs Study Start-up (RASSU) Department.Assist in compilation and revision of Regulatory Affairs (RA) documents required for clinical trials submissions.What You'll DoAssist in the contact with local study teams for RA documents collection and checks, when applicableAssist in contacting sites to obtain maintenance documents throughout the trialAssist in quality checks of documents in the study start up module and the eTMFAssist in pulling expiration reports and reconciliation reportsAssist in managing the RASSU SharePointMaintain resourcing tracker for staff assignments and future awarded workAssist is preparing site timelines for IRB reviews presented in Bid DefensesAssist in Business Intelligence (BI) report trackingAssist in preparation of study submission packages (Initial Submissions, Substantial Amendments and Non-substantial Amendments) to Ethics and Regulatory Bodies, according to countries requirementsArrange for shipments of regulatory documents and packages, track and retrieve itemsAssist in the management of the documents to be translated, when applicableAssist in SUSARs submission package preparation to Central and Local Ethics Committees in applicable countriesAssist in the preparation and completion of specific trackersAssist in applying naming conventions, upload study documentation in the study start-up module or trackers and study specific TMF system whether electronic or paper Provide backup support for RA activities, as neededProvide any other administrative support to RASSU team membersParticipate in relevant trainingsAssist in the development of Project specific Work InstructionsUpdate RASSU specialists and Directors on outstanding items, and issues as they ariseAttend weekly team meetings, prepare and distribute agendas, prepare and distribute meeting minutes, if requestedRequired Education And ExperienceBachelor’s Degree in allied health fields such as nursing, pharmacy or health/ natural science0 – 1 year of research related experience and or regulatory experienceExperience providing sound basic knowledge of medical and pharmaceutical terminologyExperience providing good understanding of the drug development and clinical trial processExperience in using Microsoft tools to edit, reformat and finalize legal regulatory documentsCOMPETENCIESExcellent verbal and written communication skillsExcellent command of English language (verbal and written)Excellent organizational and record retention skillsExcellent interpersonal skillsStrong computer skillsAbility to work independentlyAbility to handle multiple tasks and manage time efficientlyAbout CTICTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.comWhy CTI?Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.Important NoteIn light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.com email address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.Please NoteWe will never communicate with you via Microsoft Teams or text messageWe will never ask for your bank account information at any point during the recruitment process