Senior Clinical Research Specialist

Medtronic

Senior Clinical Research Specialist advancing Medtronic’s neurovascular therapies through clinical evidence generation. Authoring regulatory documents and supporting trials, publications, and submissions.

Posted 9/4/2026full-timeFridley • California, Colorado, Minnesota • 🇺🇸 United StatesSenior💰 $105,600 - $158,400 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research and regulatory writing, with a strong ability to analyze and communicate clinical data effectively. Proven experience in managing cross-functional projects within the medical device industry, particularly in neurovascular therapies.

Highest-signal resume keywords

Clinical ResearchRegulatory WritingScientific WritingClinical Data AnalysisMedical Device Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study ProtocolsClinical Study ReportsClinical Evaluation ReportsRisk-Benefit AssessmentsSubmission MaterialsLiterature ReviewsEvidence SummariesPublication PlanningData InterpretationProject Management

Soft Skills

CommunicationCollaborationStakeholder EngagementAnalytical ThinkingOrganizational Skills

Industry Keywords

Neurovascular TherapiesStrokeRegulated HealthcareLife SciencesClinical TrialsHealth EconomicsReimbursementMedical Device IndustryRegulatory SubmissionsBiomedical Science

About the role

Key responsibilities & impact

Support clinical development programs for neurovascular therapies treating stroke and other neurovascular conditions
Author and lead clinical, scientific, and regulatory documents, including clinical study protocols, clinical study reports, clinical evaluation reports, annual reports, risk-benefit assessments, and submission materials
Develop clinical evidence strategies aligned with program objectives and regulatory requirements
Partner with Clinical, Research & Development, Regulatory Affairs, Quality, Marketing, Sales, Compliance, and Health Economics & Reimbursement stakeholders
Analyze and communicate clinical data through reports, presentations, and evidence summaries
Conduct scientific literature reviews, clinical evidence assessments, and literature database management
Lead publication planning and execution with physician investigators, key opinion leaders, and internal stakeholders
Monitor and summarize emerging literature, conference presentations, and competitive developments in neurovascular therapeutics
Manage multiple clinical and business-critical projects, coordinating reviews, feedback, revisions, and approvals

Requirements

What you’ll need

Bachelor’s degree in a technical discipline and 4+ years of relevant clinical research, scientific writing, regulatory writing, or medical device experience; or an advanced degree and 2+ years of relevant experience
Experience authoring or contributing to clinical, scientific, or regulatory documentation
Experience supporting cross-functional projects within a regulated healthcare, life sciences, or medical device environment
Ability to analyze, interpret, and communicate clinical or scientific data to diverse stakeholders
Unrestricted U.S. work authorization required at the time of hire and for the duration of employment; sponsorship is not offered below Principal level
For Baccalaureate degrees earned outside of the United States, a degree satisfying 8 C.F.R. § 214.2(h)(4)(iii)(A) is required
Preferred: MD or PhD in a biomedical science discipline
Preferred: Experience supporting clinical trials and clinical development programs within the medical device industry
Preferred: Experience with clinical, medical, scientific, or regulatory writing and publication development
Preferred: Neurovascular, stroke, vascular intervention, or related medical device therapeutic area experience
Preferred: Experience supporting regulatory submissions and responses to health authorities

Benefits

Comp & perks

Competitive benefits package
Short-term incentive: Medtronic Incentive Plan (MIP)
Health insurance
Dental insurance
Vision insurance
Health Savings Account
Healthcare Flexible Spending Account
Life insurance
Long-term disability leave
Dependent daycare spending account
Tuition assistance/reimbursement
Simple Steps global well-being program
Incentive plans
401(k) plan plus employer contribution and match
Short-term disability
Paid time off
Paid holidays
Employee Stock Purchase Plan
Employee Assistance Program
Non-qualified Retirement Plan Supplement
Capital Accumulation Plan for eligible employees
Temporary employees: paid sick time as required by applicable state law
Employee Stock Purchase Plan for temporary employees