pThe 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.br/For more information, visit: /p pThe AO Innovation Translation Center (AO ITC) streamlines and drives innovation projects. Its activities include the development of clinical solutions with our industrial partner, innovation gathering, proof-of-concept studies, strategic investment in intellectual property, technology, or companies, and evidence creation through clinical research. /p pAs part of the AO ITC, Clinical Operations is the AO’s service provider for clinical research. Our clinical research specialists deliver clinical insights that are highly relevant to current surgical practice and enable better patient care by planning and conducting global clinical trials. /p h3Main Responsibilities /h3 pPublications: /p ul liConducting (systematic) literature review, review manuscript-specific literature /li liDeveloping manuscripts for submission to peer-reviewed journals according to the guidelines /li liResponsible for the entire online submission/resubmission processes /li liCritically appraise of publications and other documents /li liPrepare congress abstracts and presentations as required /li /ul pAO ITC Reports: /p ul liWriting internal reports as needed, with a main focus on study-specific final and interim reports sccording to the AO ITC CE style /li liPerform literature review as needed /li liAudit the final data analysis set in collaboration with the responsible internal partners /li /ul pAO ITC Documentation: /p ul liSupport in the development of AO ITC clinical investigation documents /li liReview and provide copy editing service as required /li /ul pCustomer Service: /p ul liSupport AO ITC CE's efforts in general, including providing English language support /li liOther ad hoc medical writing services, including supporting AO education programs /li /ul pOther: /p ul liThe 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. /li liThe employee undertakes additional responsibilities and duties as assigned by the line manager to support operational and organizational needs related to the Quality Management System. /li /ul h3Main Requirements /h3 ul liMinimally a degree in master of science in a biomedical field, preferrably an advanced degree (MD, DVM, or PhD) /li li2 - 3 years of experience in clinical research and medical writing /li liExperience with basic statistical methods (univariable tests) /li liAbility to communicate effectively /li liAttention to detail and reliability /li liAbility to work both independently and in a team /li liFlexibility and customer-focused mindset: Responsible and reliable, able to adhere to timelines /li liEnglish as native language or advanced level proficiency /li /ul #J-18808-Ljbffr
Project Manager Medical Writing, 60-100% (ID2190) Arbeitgeber: Liechtenstein Business
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