Clinical Evaluation Medical Writer

Clinical Evaluation Medical Writer Medtronic • Milan, Lombardy, Italy At Medtronic you can begin a life‑long career of exploration and innovation while helping champion healthcare access and equity for all. You'll lead with purpose breaking down barriers to innovation in a more connected compassionate world. A Day in the Life The Clinical Evaluation Medical Writer at Medtronic plays a pivotal role in the Clinical Job Family specializing in the critical review and synthesis of scientific literature. This position is designed for professionals who thrive on analyzing clinical evidence supporting regulatory submissions and contributing to the development of medical devices. As part of the Specialist Career Stream the role demands advanced education, a keen eye for detail, and the ability to work independently while collaborating with cross‑functional teams. Responsibilities Review and summarize scientific literature. Report instances of complaints/adverse events from literature to GCH. Create responses for audit/submission queries. Maintain a database of peer‑reviewed literature. Appraise, analyze, summarize, and discuss clinical evidence from all available sources. Conduct comprehensive literature searches and perform a critical evaluation of clinical evidence. Develop state of the art on product family for its intended purpose. Create & maintain plans and reports for regulatory authorities. Review/approve other documentation for device development. Have knowledge of regulatory agencies guidelines on clinical evaluation requirements. Required Knowledge and Experience Established and productive individual contributor. Works independently with general supervision on larger moderately complex projects/assignments. Set objectives for own job area to meet project objectives and contributes to milestone completion. Communicates primarily and frequently with internal contacts. External interactions are less complex, problem solving in nature. May provide guidance and assistance to entry‑level professionals and/or employees in Support Career Stream. Problem‑solving: general and may require understanding of a broader set of issues. Adopts and recommends enhancements in systems and processes to solve problems, improve effectiveness. Physical Job Requirements The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position but they are not an exhaustive list of all the required responsibilities and skills of this position. Benefits & Compensation Medtronic offers a competitive salary and flexible benefits package. This position is eligible for a short‑term incentive called the Medtronic Incentive Plan (MIP). About Medtronic We lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions. Our mission to alleviate pain, restore health, and extend life unites a global team of 95,000 passionate people. We are engineers at heart putting ambitious ideas to work to generate real solutions for real people. From the R&D lab to the factory floor to the conference room, every one of us experiments, creates, builds, improves, and solves. We have the talent, diversity, perspectives and guts to engineer the extraordinary. Key Skills Clinical Research, Adobe Acrobat, FDA Regulations, Technical Writing, Biotechnology, Clinical Development, Clinical Trials, Microsoft Powerpoint, Research Experience, Document Management Systems, Word Processing, Writing Skills Employment Type: Full-TimeExperience: YearsVacancy: 1 #J-18808-Ljbffr