What you'll do
Your role
- Clinical Trial Pipeline: Oversee the development of our clinical trial pipeline and related communication with the scientific advisory board.
- Clinical Trial Management: Lead end-to-end Clinical Trial Management, including planning, execution, CRO communication, quality assurance, budget and timeline adherence, site selection and management, data monitoring, source data verification, and submissions and communications with Ethics Committees and Competent Authorities.
- Regulatory Compliance: Ensure clinical trials follow US and EU regulations (FDA, EMA) and maintain up-to-date knowledge of regulatory requirements, and oversee all clinical investigation-related standard operating procedures.
- Data Management and Reporting: Oversee clinical data management, including collection, analysis, and reporting, provide recommendations based on trial results, and lead CRF development, database development (e.g., Castor), and the development of tools for study metrics management.
- Post-Market Clinical Follow-Up: Implement strategies to monitor product safety and performance post-market, ensuring compliance with EU MDR.
- Cross-functional Collaboration: Work with various departments (R&D, regulatory, medical) to integrate clinical research into product development.