Leica Microsystems (Schweiz) AG

Your Responsibilities: Implement, optimize, and maintain innovative microscope control applications in C# / WPF. Analyze customer requirements and design scalable and reliable state-of-the-art solutions. Continuously improve software quality and reliability by using modern tools and practices. Prepare software requirements, specifications, and architectural documentation in accordance with the company's quality standards. Become an active part of a cross functional project team and closely collaborate with internal and external stakeholders.

Your Responsibilities: Selects and manages experts and study sites. Drives, manages and executes research, pre-clinical (animal) and/or clinical studies, including post-market clinical follow-up. Authors study plans and protocols, with appropriate statistic rationales and methods of assessment, in accordance with intended clinical benefits and performance (study design). Ensures operational aspects of the studies are being conducted in accordance with all relevant ethical and government standards, Good Clinical Practices or Good Laboratory Practices, and company's procedures. Ensures submissions to regulatory competent authorities and ethics committees/IRBs, as required. On-site driving and executing studies, as required, per specific project. Analyses and discusses data and prepares study reports. Maintains a high level of professional expertise, staying abreast with scientific literature, product portfolio, and the competitive and healthcare environments. Supervises and reviews study data and documentation when collaborating with CROs. Drives process improvement initiatives which relate to the described responsibilities. Up to 50% travel.