Senior Preclinical Research Associate

Your responsibilities will include: Participate in and collaborate with POSM colleagues in the vendor selection process of preclinical test sites and their management. 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 multi-site studies. Participate in and/or lead preclinical study planning and execution, including protocol development, study execution, data analysis, interpretation, and reporting. Assist in the development of translational models by working closely with internal and external resources. Build strong, trusted relationships and contribute to cross-functional collaboration across the preclinical department and other stakeholder functions. Bachelor's degree in Biology or related field. 5+ years' experience in Preclinical or related field. Master's degree preferred. Experience in one or more of the following disciplines: Endoscopy, Urology, Neuromodulation, Cardiology, or Electrophysiology. Excellent communication, presentation, analytical, and technical writing skills. Highly motivated and able to work in a semi-independent or independent manner in a collaborative team-based environment. Knowledge of GLP regulations is desirable. Experience with regulatory body submissions, including FDA, EU MDR, PMDA, or NMPA. Proficiency with Microsoft Word, Excel, PowerPoint, Minitab, and other data analysis tools.