Clinical Development Scientist, Ultrasound &EI
Core
Executes evidence-generation processes, clinical development, and market access strategies for New Product Introduction (NPI) projects and post-market activities in the medical device sector.
Role type
Clinical Development Scientist (Medical Device)
Builds
Clinical Evaluation Reports (CERs), Clinical Study Reports (CSRs), and regulatory submissions for ultrasound and EI technologies.
Domain
Medical Devices / Ultrasound & Electromechanical Imaging
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial protocol assessment, Regulatory compliance, Clinical data analysis, Scientific literature review, New Product Introduction (NPI), Product Lifecycle Management (PLM), Clinical evidence generation strategy, Medical writing, Clinical study management, Clinical evaluation methodologies
Preferred skills
Deep domain knowledge in technology and therapeutic areas, Strategic decision-making support
Technologies
Standard software tools and systems for documentation
Responsibilities
Assess clinical trial protocols and studies to ensure alignment with regulatory standards and business objectives; Execute clinical development and market access strategies for NPI projects and post-market activities; Draft comprehensive Clinical Evaluation Reports (CERs), Clinical Study Reports (CSRs), and regulatory submissions; Troubleshoot issues related to clinical data collection, analysis, and reporting to ensure data integrity; Acquire and apply deep domain knowledge in technology and therapeutic areas to enhance clinical development activities; Produce high-quality documentation adhering to internal procedures and external regulations.
Seniority
Mid-level, hands-on IC
