Valued Team member: We are glad you are exploring new opportunities within Zimmer Biomet! What You Can Expect The Medical Writer is primarily responsible for preparing Clinical Evaluation Reports (CERs) for regulatory submissions and Post-market Surveillance Plan literature reviews (PSPs) for analysis of existing product clinical performance. Both involve conducting searches of peer-reviewed publications, national implant registries, risk management files and post market quality tabulations to compile relevant data. Report preparation involves summarizing data found and drafting risk versus benefit analyses for review by Senior Medical Writer or designee. How You'll Create Impact Identify pertinent internal and external sources of clinical data and conduct systematic literature searches of peer review publications. Prepare Clinical Evaluation documents according to the applicable regulations (including MDR (EU) 2017/745) and Zimmer Biomet internal procedures using relevant information compiled from clinical research, peer reviewed publications, risk management files and post market data. Summarize findings and draft risk versus benefit analyses and conclusions, for review by Medical Writing Manager or designee, based on clinical and post market data. Distribute reviewed final draft reports to Clinical Affairs, Regulatory Affairs, Post-Market Surveillance and Development Engineering groups to verify and approve content of final draft document. Prepare reviews of peer-reviewed literature for inclusion in Zimmer Biomet post-market surveillance (PMS) reports. Support the Manager or Team Leader for Audit activities including the participation in Audits as clinical evidence SME as needed File work in the Clinical Evaluation archives, provide clinical data searches and documentation as a service to various functions within Zimmer Biomet, and provide verbal and/or written progress reports monthly. What Makes You Stand Out - Proficient in English – written and spoken B2 - Excellent written and verbal communications skills - Demonstrated technical and medical writing competence - Understanding of statistical methods - Ability to critically analyze and interpret scientific data - Ability to work within tight deadlines, adjust to changes in priorities - Takes actions that are best for the company versus his or her individual unit - Encourages and supports information sharing and collaboration across teams and departments - Demonstrates sound business ethics; shows consistency among principles, values and behaviors. - Strong ability to interpret and disseminate relevant clinical studies / medical product information. - Basic understanding of regulatory compliance for medical devices. Your Background - Your CV has to be in english mandatory. - Minimum of a Bachelor’s degree or equivalent education in health, life sciences, engineering or a similar discipline required. MD, MS and PhD preferred. - Demonstrated authorship of scientific publications in peer review journals will be an asset. - 2-5 years of experience in medical writing, clinical affairs, regulatory affairs, or product engineering in the medical device industry required, with a strong preference to those with similar work experience in the orthopedic medical device industry. - In lieu of the medical device industry experience, 3-5 years as a professor or senior investigator in a healthcare related field, with a demonstrated record of research and scientific publications. Travel Expectations 5% EOE/M/F/Vet/Disability #J-18808-Ljbffr