PAt 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. /pbA Day in the Life /b Medtronic is looking for a Biostatistician to join our Medtronic Clinical and Regulatory Solutions (MCRS) team. In this role, you will apply statistical expertise along with SAS and R programming skills to support global clinical research initiatives. Working closely with our Statistical Programming team, you will contribute to generating high-quality clinical evidence, including analysis of real-world hospital data.brReporting to the Manager of Biostatistics, you’ll be part of a collaborative team focused on delivering innovative and effective clinical solutions. This position has a hybrid working model, with smart working with a preference for candidates based in Rome.pbResponsibilities may include the following and other duties may be assigned: /b /pulliApply biostatistical methods to support research and development plans for medical device products /liliContribute statistical expertise throughout the product life cycle /liliAnalyze data to support statistical inference, and assist in developing tables, graphs, and study reports /liliCollaborate with clinical teams and provide guidance to statistical programmers /li /ulpbRequired Knowledge and Experience: /b /pulliBachelor’s degree in Statistics or related field required, Master’s Degree is preferred /liliA minimum of 2 years of experience in clinical trial design and/or clinical data analysis within the healthcare industry, academia, or research organization; or a relevant advanced degree with at least 1 year of related experience within biopharma or medical device indesty /liliProficiency in SAS and R programming /li /ulpThe ideal candidate would hold a Master’s degree in Biostatistics, Statistics, or Epidemiology and have at least two years of experience in statistics within a Clinical Research Organization, the Medical Device Industry or Biopharma. Familiarity with Good Clinical Practice and regulatory compliance guidelines for clinical trials and medical devices, such as ISO and MDR, is valuable. A solid understanding of research data management and relational databases, along with strong proficiency in Microsoft Office tools, particularly Word and Excel, is important. The role also benefits from the ability to communicate complex statistical concepts to non-specialists, strong interpersonal and collaboration skills, and a proactive, adaptable attitude in dynamic and evolving environments. /ppbPhysical Job Requirements /bbrThe 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. /pbBenefits Compensation /bpbMedtronic offers a competitive Salary and flexible Benefits Package /bbrA commitment to our employees lives at the core of our values. We recognize their contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage.br/pbAbout Medtronic /bpWe lead global healthcare technology and boldly attack the most challenging health problems facing humanity by searching out and finding solutions.brOur Mission — to alleviate pain, restore health, and extend life — unites a global team of 95,000+ passionate people.brWe are engineers at heart— putting ambitious ideas to work to generate real solutions for real people. From the RD lab, to the factory floor, to the conference room, every one of us experiments, creates, builds, improves and solves. We have the talent, diverse perspectives, and guts to engineer the extraordinary. /ppLearn more about our business, mission, and our commitment to diversity ahere /a br/p #J-18808-Ljbffr