Senior Medical Science Writer

We anticipate the application window for this opening will close on - 16 Oct 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 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 our cross-functional collaboration efforts. This role will require 10% of travel to enhance collaboration and ensure successful completion of projects. Within the clinical science and evidence team, part of the CRM Clinical Research and Medical Affairs organization, one of our responsibilities includes management of the scientific publication process and global evidence dissemination from Medtronic-sponsored clinical trials, registries, and other research data. In this role, the Senior Medical Science Writer will work closely with Principal Investigators and internal team members from the clinical study team, statistics, clinical leadership and cross-functional SMEs. With the growing volume of data, rapid advances in AI, and continuous innovation in technology, we are at a pivotal moment to reimagine how scientific evidence is disseminated. As access to information becomes commoditized – easy, fast, and inexpensive – our ability to understand and impact humanity becomes more critical than ever. This role will collaborate across internal and external partners to define and execute scientific dissemination strategies. The primary focus will be to identify channels, formats, and content that tailor scientific and medical results and data by audience segment, based on expertise, literacy, and needs. The medical communication professional will use a range of techniques to assess understanding and increase engagement. Responsibilities: Translate complex scientific and medical information into clear, accessible language for diverse audiences, including clinicians, healthcare providers, patients, caregivers, and regulators. Develop and implement data-driven scientific evidence communication strategies that align with dissemination goals, audience needs and preferred formats and channels – maximizing our evidence footprint through ‘Evidence for Action’. Conduct audience analysis to define the needs, interests, and knowledge level of the target recipients. Create high-quality medical and scientific content, including manuscripts, abstracts, presentations, plain language summaries, graphical abstracts, white papers, and other innovative formats. Tailor writing style, tone, and level of detail to ensure content is appropriate and engaging for each audience. Manage the project timeline for each deliverable through final delivery (e.g. peer-review publication, scientific conference presentation) ensuring compliance to regulatory, medical society, and corporate standards. Interface with physicians, clinical leadership, and other stakeholders to align evidence dissemination activities and deliverables Maintain an in-depth knowledge of key therapy and product areas, stay abreast of current literature relevant to CRM therapies and products (including competitors) Collaborate with subject matter experts, such as researchers, clinicians, and regulatory affairs, to gather information and ensure accuracy. Must Have: Minimum Requirements To be considered for this role, please ensure the minimum requirements are evident in your applicant profile. Bachelor’s degree required Minimum of 4 years of clinical/medical/scientific writing experience Or advanced degree with a minimum of 2 years clinical/ medical/ scientific writing experience Nice to Have Advanced degree in life sciences, medicine, or a related field (e.g., MS, MD, PharmD, PhD). Demonstrated ability to write for various audiences with different levels of scientific understanding. Demonstrated knowledge of physiology and/or applicable disease states, medical terminology, CRM therapies and technologies Experience authoring peer-reviewed manuscript and abstract presentations at major scientific conferences Proven track record of developing clear and concise documents. Excellent organizational and project management skills. Proven track record of excellent writing skills (medical writing certification is a plus: CMPP, BELS, AMWA, MWC) Excellent interpersonal, presentation, and communication skills 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 enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment. ‌ Recruitment Fraud Alert We are aware of phishing scams targeting job seekers. 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