Preclinical Research Associate II

Your responsibilities will include: Collaborate with POSM colleagues on the selection and management of external preclinical test sites. Provide oversight and serve as a liaison during study execution to ensure study integrity, timelines, and budgets are met and communicated to appropriate stakeholders, including for multisite studies. Participate in and, as appropriate, lead preclinical study planning and execution, including protocol development, study conduct, data analysis, interpretation, and reporting. Support the development of translational models to meet project or corporate objectives by partnering with internal and external resources. Build strong, trust-based relationships and contribute to collaboration across the preclinical department and with cross-functional partners. Bachelor's degree in biology or a related field. Minimum of 0 to 3 years' experience in a preclinical or related field. Experience in one or more of the following disciplines: endoscopy, urology, neuromodulation, cardiology, or electrophysiology. Strong communication, presentation, analytical, and technical writing skills. Highly motivated self-starter with the ability to work independently or semi-independently in a collaborative, team-based environment. Knowledge of Good Laboratory Practice regulations. Experience supporting regulatory submissions to bodies such as the FDA, EU MDR authorities, PMDA, or NMPA. Proficiency with common computer and data analysis tools, including Word, Excel, PowerPoint, Minitab, and other statistical or data analysis software.