Jobs / United States / Medtronic INC
Senior Medical Science Writer
Medtronic INC · 🇺🇸 Dallas, Texas, United States of America
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 193 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 106 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Medtronic INC paid sponsored hires in similar roles1 certified filing for “Pr. AI Data Science Engineer” (Molecular and Cellular Biologists) in CA: $127k–$127k, median $127k. Most were filed at wage level IV (100%) — 4 lottery entries, ≈61% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
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Sponsor Radar — Medtronic INC
The US Department of Labor certified 193 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 106 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Medtronic INC →
About the role
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,