Project Manager Medical Writing, 60-100%

h3bProject Manager Medical Writing, 60-100% /b /h3 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 h3Project Manager Medical Writing, 60-100% (ID2190) /h3 pbMain Responsibilities /b /p 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 pbMain Requirements /b /p 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 liAn interesting and varied job in an exciting and innovative organization /li liThe opportunity to be part of a highly committed international team /li liModern infrastructure /li liHigh degree of flexibility regarding working hours and location (depending on operational requirements) /li liGenerous pagacke of social benefits, including supplementary vacation days and pension scheme contributions /li liInternal skills training opportunities and support for continued education /li /ul pjid6b33f96jm jit1041jm jiy26jm /p ul libWork location /b 7205 Zizers (GR) /li libWorkload /b 60% - 100% /li libEmployment start /b By agreement /li libEmployment duration /b Permanent /li libBy online /b Online form /li /ul #J-18808-Ljbffr