Project Manager Medical Writing, 60-100%

Project Manager Medical Writing, 60-100% (ID2133)brThe AO is a medically guided, not-for-profit organization, a global network of surgeons, and the world's leading education, innovation, and research organization specializing in the surgical treatment of trauma and musculoskeletal disorders. We are home to people from all over the world, from different backgrounds, with diverse talents and specialist areas. What binds us together is our passion for excellence, our dedication to our mission of improving patient care, and our understanding that we are stronger together: we are one AO.brFor more information, visit: /brProject Manager Medical Writing, 60-100% (ID2133)brMain ResponsibilitiesbrPublications:brConducting (systematic) literature review, review manuscript-specific literaturebrDeveloping manuscripts for submission to peer-reviewed journals according to the guidelinesbrResponsible for the entire online submission/resubmission processesbrCritically appraise of publications and other documentsbrPrepare congress abstracts and presentations as requiredbrAO ITC Reports:brWriting internal reports as needed, with a main focus on study-specific final and interim reports sccording to the AO ITC CE stylebrPerform literature review as neededbrAudit the final data analysis set in collaboration with the responsible internal partnersbrAO ITC Documentation:brSupport in the development of AO ITC clinical investigation documentsbrReview and provide copy editing service as requiredbrCustomer Service:brSupport AO ITC CE's efforts in general, including providing English language supportbrOther ad hoc medical writing services, including supporting AO education programsbrOther:brThe employee performs all tasks in alignment with the requirements of the ISO 9001 quality management standard and actively contributes to maintaining and improving the quality system.brThe employee undertakes additional responsibilities and duties as assigned by the line manager to support operational and organizational needs related to the Quality Management System.brMain RequirementsbrEducation:brMinimally a degree in master of science in a biomedical field, preferrably an advanced degree (MD, DVM, or PhD)brJob specification:br2 - 3 years of experience in clinical research and medical writingbrExperience with basic statistical methods (univariable tests)brAbility to communicate effectivelybrAttention to detail and reliabilitybrAbility to work both independently and in a teambrFlexibility and customer-focused mindset: Responsible and reliable, able to adhere to timelinesbrEnglish as native language or advanced level proficiencybrAn interesting and varied job in an exciting and innovative organizationbrThe opportunity to be part of a highly committed international teambrModern infrastructurebrHigh degree of flexibility regarding working hours and location (depending on operational requirements)brGenerous pagacke of social benefits, including supplementary vacation days and pension scheme contributionsbrInternal skills training opportunities and support for continued education jidc3f27a7a jit0832a jiy26a