About this role
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 according 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, preferably 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