Clinical Research Specialist - Remote

We anticipate the application window for this opening will close on - 21 May 2026 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 As one of three comprehensive portfolios at Medtronic, Neuroscience is dedicated to improving the lives of people living with neurological disorders, spine conditions, and chronic pain. Guided by our Mission—to alleviate pain, restore health, and extend life—we develop technologies and therapies that help people regain function, reduce pain, and return to the activities that matter most. Our Cranial & Spinal Technologies (CST) Operating Unit develops and delivers an integrated ecosystem of spinal implants, navigation and robotic guidance systems, advanced imaging, and data-driven planning tools for complex spine and cranial procedures. Platforms such as AiBLE™ connect these technologies to enhance surgical precision, streamline workflows, and support improved patient outcomes worldwide. Check us out on LinkedIn: Medtronic CST The Clinical Research Specialist supports clinical evidence strategy across the product lifecycle, with a primary focus on leading New Product Innovation (NPI) clinical evidence generation activities and managing Post‑Market Clinical Follow‑up (PMCF) activities in accordance with EU MDR requirements. This is a strategy‑driven role, responsible for clinical evidence planning, execution, assessment, and documentation. The position does not perform day‑to‑day clinical operations but works closely with Clinical Operations and cross‑functional teams across the Cranial & Spinal Technologies (CST) operating unit to ensure clinical data collection activities are aligned with regulatory and business needs. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. This position is remote to enhance our competitive edge and expand cross-functional collaboration. This role will require some travel to enhance collaboration and ensure the successful completion of projects. Responsibilities may include the following and other duties may be assigned. Lead clinical evidence strategy for the CST portfolio, including development and maintenance of Global Clinical Evidence Strategy (GCES) documentation aligned to business needs. Develop, maintain, and periodically revise PMCF Plans in accordance with EU MDR Annex XIV; assess evidence sufficiency and execute PMCF activities (surveys, registries, observational studies) to close identified gaps. Integrate PMCF outputs into CERs and related documentation; evaluate the impact of incremental product changes on PMCF strategy. Partner with Clinical Operations on PMCF study design, and with Medical Writing on CEPs, CERs, PMCFRs, and SSCPs. Collaborate with Regulatory Affairs, Quality, R&D, Medical Affairs, and Marketing on submissions, post-market assessments, and claims substantiation. Support responses to Notified Body and regulatory authority inquiries; support surgeon engagements as needed. Maintain strategic oversight of PMCF activities and ensure all documentation remains current, traceable, and audit-ready. Required Knowledge and Experience: Baccalaureate degree Minimum of 2 years of relevant experience, or an advanced degree with 0 years of experience. Nice to have: Experience with EU MDR PMCF activities Familiarity with medical device clinical documentation (PMCF, CER, CEP) Exposure to regulatory or audit support Strong cross‑functional collaboration skills High level of attention to detail in regulated environments For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. 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. The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role. U.S. Work Authorization & Sponsorship At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our