Clinical Affairs Project Manager

Robeauté is redefining the future of brain therapies through the first microrobotic platform designed to navigate the human brain with unprecedented precision. This new generation of medical microrobots will be able to diagnose, treat, and monitor the brain from within, overcoming the persistent limitations in treating neurological diseases that affect more than one in three people worldwide. Since its founding in 2017, Robeauté has filed more than 50 patent applications. We recently raised €27 million in a Series A round led by Plural, Cherry Ventures, Kindred Ventures, and Brainlab, fueling our next phase of growth. The successful candidate must excel in an energetic, collaborative small team environment, be able to move seamlessly between medical and engineering cultures and have a commitment to high product quality and scientific integrity. A strong sense of shared responsibility and shared reward is required, as is the ability to make work fun and interesting. The Clinical Affairs Project Manager has the responsibility of planning, organizing and executing the GLP preclinical and early clinical studies with Robeauté’s robotic brain biopsy and local drug delivery device, including support of regulatory submissions for clinical studies across geographies, IDE submission to the FDA , reporting to Head of Clinical. In particular, the Clinical Affairs Project Manager will plan and coordinate the preclinical and clinical studies together with the Head of Clinical and surgeon collaborators. The responsibilities include: Preclinical and clinical study design (including GLP animal studies and animal model exploration ) Writing preclinical and clinical protocols Preparing documentation for submission to local Ethics Committees, competent authorities in various geographies including to the US FDA (IDE) Clinical study site contracting CRO selection and contracting, including management of both GLP preclinical studies and clinical studies. Communication and collaboration wi