
10,000+ employees
Founded 1941
⚕️ Healthcare Insurance
🧬 Biotechnology
Healthcare Insurance • Medical Devices • Biotechnology
Stryker is a global leader in medical technology, providing innovative products and services across the healthcare sector. With a presence in countries across the Americas, Asia Pacific, Europe, and the Middle East & Africa, Stryker offers a wide range of medical technologies, including orthopedic implants, surgical equipment, and advanced hospital devices. The company is committed to improving patient outcomes and healthcare efficiency. Stryker continues to expand its global reach, offering localized solutions to meet diverse healthcare needs worldwide.
🔥 3 minutes ago
🚗 Michigan – Remote
💵 $126.5k - $273.9k / year
⏰ Full Time
🟠 Senior
🔴 Lead
🧪 Clinical Research
🦅 H1B Visa Sponsor
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10,000+ employees
Founded 1941
⚕️ Healthcare Insurance
🧬 Biotechnology
Healthcare Insurance • Medical Devices • Biotechnology
Stryker is a global leader in medical technology, providing innovative products and services across the healthcare sector. With a presence in countries across the Americas, Asia Pacific, Europe, and the Middle East & Africa, Stryker offers a wide range of medical technologies, including orthopedic implants, surgical equipment, and advanced hospital devices. The company is committed to improving patient outcomes and healthcare efficiency. Stryker continues to expand its global reach, offering localized solutions to meet diverse healthcare needs worldwide.
• Develop and implement clinical research strategies aligned with Surgical Technology priorities and compliance standards. • Collaborate with regulatory, marketing, and health economics teams to align clinical evidence with product claims and reimbursement requirements. • Lead end-to-end clinical studies, including protocol development, site selection, contracting, monitoring, data collection, and study close-out to meet timelines and quality targets. • Conduct investigator meetings and ensure protocol adherence and study readiness prior to trial initiation. • Manage clinical research budgets, track spend vs. plan and deliver studies within approved financial and timeline parameters. • Oversee and evaluate contract research organizations by monitoring deliverables, budgets, and resource allocation. • Produce and review clinical documentation, including study reports, publications, and evidence-based materials supporting commercial activities. • Maintain compliance with Good Clinical Practice (ISO 14155), applicable regulations, and internal procedures through audits, monitoring, and documentation control.
• Bachelor's degree in a science or research-based field (e.g., natural sciences, nursing, engineering) • Minimum 8 years of clinical or basic research experience in a medical-related field • Demonstrated working knowledge of Good Clinical Practice (ISO 14155) and medical device clinical study standards • Proven experience developing and managing clinical studies from initiation through publication • Documented experience with scientific publication and/or conference presentations • Preferred Postgraduate degree (e.g., Master’s or PhD) in a related discipline • Experience in medical device clinical research • Experience in surgical technologies, general surgery, obstetrics, or related clinical areas • Experience in scientific or medical writing for publications or regulatory documentation.
• Health insurance • 401(k) plan • Paid time off • Remote work options
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