Senior Clinical Research Specialist

• Execute and oversee global clinical studies in the Surgical Operating Unit
• Oversee, design, plan, and develop clinical evaluation research studies
• Prepare and author protocols and patient record forms
• Conduct registered and non-registered clinical studies
• Oversee and interpret clinical investigation results for new drug, device, or consumer applications
• Oversee and resolve clinical trial operational aspects with project teams
• Prepare clinical trial budgets as needed
• Manage clinical supplies operations, site selection, and vendor selection as needed
• Assume project management responsibilities for selected studies and site management activities
• Represent Medtronic from a clinical research perspective within the country or region
• Collect feedback from local customers and authorities
• Build and maintain relationships and collaborations with internal and external parties
• Drive local evidence dissemination and awareness
• Mentor colleagues or direct the work of lower-level professionals as needed

• Bachelor's degree required
• Minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years of relevant experience
• Knowledge of Medtronic systems
• Understanding of clinical Quality and Regulatory environments
• Experience in the medical device industry
• For baccalaureate degrees earned outside the United States, a degree satisfying 8 C.F.R. § 214.2(h)(4)(iii)(A) is required
• Unrestricted U.S. work authorization at the time of hire and for the duration of employment

Demonstrates expertise in executing and overseeing global clinical studies, with a strong focus on clinical evaluation research, project management, and regulatory compliance in the medical device industry. Capable of building relationships and mentoring team members while managing clinical trial operations and budgets.

• Clinical Study Management
• Project Management
• Clinical Evaluation Research Regulatory Compliance
• Medical Device Industry Experience

• Protocol Preparation
• Clinical Trial Budgeting
• Clinical Investigation Interpretation
• Clinical Supplies Management
• Site Selection
• Vendor Selection
• Data Analysis
• Clinical Trial Operations

• Relationship Building
• Mentoring
• Collaboration
• Communication

• Clinical Research
• Surgical Operating Unit
• Quality and Regulatory Environments
• Clinical Trials
• Evidence Dissemination

• Medtronic Systems