Medtronic is looking to solve clinical study and data management issues in Acute Care and Monitoring by developing protocols, executing studies, managing data, and analyzing data.
Requirements
- Experience with programming languages including Python and Matlab
- Medical device development experience, design control, FDA and MDR regulations.
- Experience in data science and analysis.
- General knowledge of related principals including electromechanical, tissue optics, physiological signals, etc.
- Experienced in design for six sigma or similar engineering practices
- Experience with pulse oximetry/light-based sensing
- Knowledge of regulatory requirements (FDA, IEC, ISO) and quality management systems.
Responsibilities
- Provides technical support to clinical study sites by serving as the technical resource between engineering and the medical community.
- Support research and development in evaluating concepts of new products and modifying existing devices or therapies.
- Collaborates with various departments on the design, documentation, testing, and implementation of clinical data collection studies, and clinical database review.
- Assist with design and implementation of clinical protocols and data collection systems.
- Develops systems for organizing data to analyze, identify and report data and trends.
- Manages data management issues by reviewing protocols for cross-project consistency, and identifying standard Case Report Form (CRF) modules to meet objectives.
- Review and resolve data discrepancies for standardized data validation systems and procedures.
Other
- Bachelor’s degree required
- Minimum of 4 years of relevant experience, or a Master's degree with a minimum of 2 years of relevant experience.
- Travel Requirements: 10 – 25%
- Strong time and project-management skills with a high attention to detail.
- Excellent problem-solving, analytical, and critical thinking abilities.
