Jobs / United States / Medtronic INC
Clinical Research Spec
Medtronic INC · 🇺🇸 Mounds View, Minnesota, 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 “Clinical Manager” (Computer and Information Systems Managers) in FL: $127k–$127k, median $127k. 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 - 13 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 The ICT portfolio delivers differentiated cardiovascular technologies that help clinicians detect and manage cardiac conditions earlier, treat patients more effectively, and improve outcomes. By combining advanced device innovation, actionable data, and connected care capabilities, the portfolio supports better clinical decision-making and creates value for patients, providers, and healthcare systems. At Medtronic, we bring bold ideas forward with speed and decisiveness to put patients first in everything we do. In-person exchanges are invaluable to our work. We’re working a minimum of 4 days a week onsite as part of our commitment to fostering a culture of professional growth and cross-functional collaboration as we work together to engineer the extraordinary. This position will be based in Mounds View, MN. In this exciting role as a Clinical Research Specialist within the Interventional Cardiology Therapies (ICT) Operating Unit, you will have primary focus and responsibility for study execution and clinical study site management on a key clinical program to support the development and advancement of best-in-class ICT device-based technologies. You will work under the direction and closely with the Clinical Study Manager to satisfy applicable regulatory standards and Medtronic internal requirements for clinical studies. • Reviews and approves required documents for study start, assures continued validity of such documents, takes actions for updates and/or replacements, and monitors site activation • Performs site initiation activities, resolution and follow-up of site issues, and study closure activities. • Provides support and training for clinical study sites to assure data integrity and protocol compliance. • Prepares study materials and/or training and tracks and maintains study documentation. • Sets up and maintains accurate clinical study files. • Coordinates activities of associates (assigned clinical site staff) and investigators to ensure compliance with CIP and overall clinical objectives • Perform site file reviews • Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), Good Clinical Practice (GCP) and specific country regulations and may prepare clinical trial budgets. • Participates in overall clinical management plan, protocol and case report form development. • Performs data review, reviews data discrepancies, ensures data queries are being resolved, works closely with monitors to ensure monitoring action items are resolved, and generates reports. • Reports on progress and results of clinical investigations • May be responsible for clinical supply operations, site and vendor selection. • Builds and maintains optimal relationships and effective collaborations with various internal and external parties. • Assists clinical management with other duties as requested. Must Have (Minimum Requirements): To be considered for this role, the minimum requirements must be evident on your resume. • Bachelor's degree and a minimum of 2 years of clinical research experience • Or advanced degree with 0 years of experience Nice to H