Senior Staff Clinical Scientist @ Stryker
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Overview
Stryker is seeking a Senior Staff Clinical Scientist to join our Neurovascular Division. You can be based in Fremont, CA or work remotely from anywhere within the United States.
What You Will Do
You will represent the Clinical Science function on project and study teams to develop clinical evidence strategies and deliverables related to studies. Responsibilities include project managing clinical deliverables, producing study plans, reports, clinical evaluation and post-market follow up plans, regulatory submissions, and real world evidence protocols. You will provide clinical subject matter expertise to internal stakeholders and assist in developing junior team members across clinical science and medical writing disciplines.
Required Qualifications
- Bachelor’s Degree in a health or science-related field.
- 6+ years combined experience in clinical research, medical writing, and clinical science.
- Previous medical writing experience in the healthcare product or medical device industry.
- Strong analytical skills and ability to process complex scientific data.
- Excellent knowledge of regulatory guidelines (FDA/CFR; EN540/MDR/GCP) and quality standards (ISO 14155/14971).
Preferred Qualifications
- Advanced degree (MSc, MPH, PhD) in a related field.
- Experience in research study design and publication writing.
- Knowledge in vascular space and IDE/Class III products clinical trials.
- Familiarity with AMWA code of ethics and guidelines.
Compensation & Benefits
Salary ranges between $100,500 and $215,300 plus bonus eligibility and a competitive benefits package including health, financial, and wellness programs.
Key skills/competency
- Clinical Science
- Medical Writing
- Regulatory Guidelines
- Project Management
- Evidence Strategy
- Neurovascular
- Clinical Research
- Data Analysis
- Study Design
- Stakeholder Collaboration
How to Get Hired at Stryker
🎯 Tips for Getting Hired
- Research Stryker's culture: Study their mission, values, and product news.
- Customize your resume: Highlight clinical research and regulatory expertise.
- Prepare for interviews: Emphasize medical writing and project management skills.
- Showcase technical aptitude: Provide examples of strategic clinical evidence projects.