Project Manager Medical Writing, 60-100% (ID2190)

Job description

Main Responsibilities Publications: Conducting (systematic) literature review, review manuscript-specific literature Developing manuscripts for submission to peer-reviewed journals according to the guidelines Responsible for the entire online submission/resubmission processes Critically appraise of publications and other documents Prepare congress abstracts and presentations as required AO ITC Reports: Writing internal reports as needed, with a main focus on study-specific final and interim reports sccording to the AO ITC CE style Perform literature review as needed Audit the final data analysis set in collaboration with the responsible internal partners AO ITC Documentation: Support in the development of AO ITC clinical investigation documents Review and provide copy editing service as required Customer Service: Support AO ITC CE's efforts in general, including providing English language support Other ad hoc medical writing services, including supporting AO education programs Other: The 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. The employee undertakes additional responsibilities and duties as assigned by the line manager to support operational and organizational needs related to the Quality Management System. Main Requirements Minimally a degree in master of science in a biomedical field, preferrably an advanced degree (MD, DVM, or PhD) 2 - 3 years of experience in clinical research and medical writing Experience with basic statistical methods (univariable tests) Ability to communicate effectively Attention to detail and reliability Ability to work both independently and in a team Flexibility and customer-focused mindset: Responsible and reliable, able to adhere to timelines English as native language or advanced level proficiency