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Medical Writer
3 miesięcy temu
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.
As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talent team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels included, respected, empowered, and recognized.
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. The scope includes products of Reconstruction, Trauma and Biologics Divisions.
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 Excellent written and verbal communications skills. Demonstrated technical and medical writing competence. Strong organizational skills, attention to detail and proofreading skills. Understanding of statistical methods Ability to critically analyze and interpret scientific data Have an analytic and strategic mindset Ability to work within tight deadlines, adjust to changes in priorities Ability to function independently Ability to identify problems and research possible solutions 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. Proficiency in MS Office applications and proficiency in or ability to learn EndNote or Reference Manager or other similar software tools needed for performing the job. Basic understanding of regulatory compliance for medical devices.
Your Background
Minimum of a Bachelor’s degree or equivalent education in health, life sciences, engineering or a similar discipline required. MS and PhD preferred. Demonstrated authorship of scientific publications in peer review journals will be an asset. 3-5 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.EOE/M/F/Vet/Disability
