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 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