[Remote] Trial Master Files Representative
Note: The job is a remote job and is open to candidates in USA. Celerion is committed to swift, exceptional clinical research through translational medicine. In this role, you will be involved in the preparation and maintenance of Trial Master Files for studies, ensuring compliance with protocol and regulatory requirements.ResponsibilitiesInvolved in the preparation and the completeness of the Trial Master Files (TMF) for internal and external studiesResponsible for maintenance of the TMF, creating a file structure and indexing contentsCommunicate with client Sponsors, Project Managers, monitors, sites and other study contacts to ensure compliance to protocol, and regulatory/local requirementsSkillsBachelor's degree in related field such as science, nursing, or other biomedical disciplineMinimum 1 year document management experienceExcellent interpersonal and oral/ written communication skillsHighly organized and collaborativeProficient computer skills, i.e., MS Word, Excel, PowerPointAbility to manage multiple prioritiesExperience in clinical research and/or Trial Master Files preferredCompany OverviewCelerion, a leader in early clinical research, delivers Applied Translational Medicine. It was founded in 2010, and is headquartered in Lincoln, Nebraska, USA, with a workforce of 1001-5000 employees. Its website is https://celerion.com/.