Senior Clinical Research Specialist - NV - Irvine, CA; Lafayette, CO or Fridley, MN (Onsite)

We anticipate the application window for this opening will close on - 12 Sep 2026   Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the Life The Neurovascular Clinical Research team supports the global clinical development of therapies designed to treat stroke and other neurovascular conditions. This team partners across Clinical, Research & Development, Regulatory, Quality, Health Economics & Reimbursement, Marketing, and Medical Affairs to generate clinical evidence that supports product development, regulatory submissions, and commercialization activities. Primary preference is for candidates based in Fridley/Mounds View, Minnesota OR Irvine, California OR Lafayette, Colorado. This role follows a flexible onsite work model with a minimum of four days per week onsite. Travel requirements are expected to be ~25% based on business needs.                     Check us out on LinkedIn: Medtronic Neurovascular The Senior Clinical Research Specialist supports clinical development programs by leading the development of clinical, scientific, and regulatory documentation while partnering with cross-functional stakeholders to advance evidence generation strategies. This role contributes to study start-up, study execution, publication planning, regulatory submissions, and broader clinical development initiatives supporting neurovascular therapies.

Author and lead the development of clinical, scientific, and regulatory documents, including clinical study protocols, clinical study reports, clinical evaluation reports, annual reports, risk-benefit assessments, and associated submission materials. Develop clinical evidence strategies and support clinical development activities aligned with program objectives and regulatory requirements. Partner with cross-functional stakeholders across Clinical, Research & Development, Regulatory Affairs, Quality, Marketing, Sales, Compliance, and Health Economics & Reimbursement to support product development and lifecycle initiatives. Interpret, analyze, and communicate clinical data through clear and scientifically accurate reports, presentations, and evidence summaries for internal and external audiences. Conduct scientific literature reviews, clinical evidence assessments, and literature database management activities to support development and regulatory objectives. Lead publication planning and execution activities in collaboration with physician investigators, key opinion leaders, and internal stakeholders. Monitor and summarize emerging scientific literature, conference presentations, and competitive developments relevant to the neurovascular therapeutic area. Manage multiple clinical and business-critical projects simultaneously, coordinating document reviews, stakeholder feedback, revisions, and approval processes.

Bachelor’s degree in a technical discipline and 4+ years of relevant clinical research, scientific writing, regulatory writing, or medical device experience; or an advanced degree and 2+ years of relevant experience. Experience authoring or contributing to clinical, scientific, or regulatory documentation. Experience supporting cross-functional projects within a regulated healthcare, life sciences, or medical device environment. Ability to analyze, interpret, and communicate clinical or scientific data to diverse stakeholders.

MD or PhD in a biomedical science discipline. Experience supporting clinical trials and clinical development programs within the