Role Description 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. - Plan and coordinate the preclinical and clinical studies together with the Head of Clinical and surgeon collaborators. - 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 with surgeon KOLs on study design, protocols and their execution. - Data collection and data management after testing. - Writing of detailed reports after preclinical or clinical use based on the data collected. - Planning and participation in conferences, medical scientific communication and publication support. In parallel, the Clinical Affairs Project Manager is expected to gain detailed knowledge of the clinical applications of Robeauté’s device and connect with and curate surgeon relationships with the goal of growing the surgeon community with mutual respect. The Clinical Affairs Project Manager will collaborate with the technical team that designs hardware and software by giving feedback after any device use in a preclinical or clinical context, on the robot’s performance and in order to develop the platform’s performance with an eye for the global development of the platform. Furthermore, the Clinical Affairs Project Manager will collaborate with Head of Clinical on Medical Affairs management, the representation of Robeauté’s platform at conferences, the creation of a publication pipeline and the medical scientific value communication within the surgeon community. This role is open to candidates based in EMEA locations. Qualifications - MD, Master’s or Ph.D. in a Life Sciences field, Biomedical Engineering and/or M.Eng. and equivalent work experience in relevant areas. - At least 5 years experience in preparation and execution of clinical trials with medical devices, including preclinical (GLP) and/or regulatory submissions (IDE preferred) and subsequent study execution. - Device test experience in lab and clinical environments. - Good written, communication and documentation skills in English required and French preferred. Requirements - Good knowledge of anatomy and physiology and ability to relate to surgeons and the surgeon community. - Ability to communicate Robeauté's product and mission to the surgeon community. - Good ability and predisposition for teamwork as well as ability to work independently. - Strong interdisciplinary understanding of robotics, electronics and control.

Role Description We are looking for an experienced OnBase Project Manager to lead enterprise content management (ECM) projects using Hyland OnBase. The ideal candidate will: - Manage project planning, timelines, budgets, resources, and stakeholder communication while ensuring successful delivery. - Collaborate with business users, technical teams, and vendors to gather requirements, mitigate risks, and drive project execution. Experience with OnBase implementations, workflow automation, document management, integrations, and system upgrades is required. Strong knowledge of Agile and Waterfall methodologies, excellent leadership, communication, and problem-solving skills are essential. PMP certification and healthcare, insurance, or financial services experience are preferred. This is a remote position. Qualifications - Experience with OnBase implementations - Strong knowledge of Agile and Waterfall methodologies - Excellent leadership, communication, and problem-solving skills - PMP certification preferred - Experience in healthcare, insurance, or financial services preferred Requirements - Manage project planning, timelines, budgets, and resources - Ensure successful delivery of ECM projects - Collaborate with business users, technical teams, and vendors - Gather requirements and mitigate risks - Drive project execution Benefits - 401(k) - Dental insurance - Vision insurance

• Lead healthcare facility outfitting or construction projects, overseeing planning, coordination, and execution. • Demand strong leadership, contract management, and field coordination skills. • Ensure project milestones are met, requiring 50%+ travel for onsite installations.

• Implementation of our software solutions in museums, collections, galleries and archives (focus: Benelux, then broader Europe) • Planning, execution, management and control of customer projects of various sizes within a multi-project environment, meeting time and budget targets • Demonstrating standard features, highlighting functional possibilities and clarifying the boundaries with customizations • When required, analyzing extended customer requirements and specifying modifications. Implementation together with our technical experts through configuration and code extensions • Implementing add-ons and new product releases for existing customers (modules, apps, online publications) • Leading data migrations of limited complexity or managing self-configured data imports via our standard interface • Defining work packages, assigning project teams and ensuring delivery quality by conducting release tests, organizing customer tests (UAT) and overseeing project acceptance • Effective communication with stakeholders and Customer Care is central; conducting project meetings, workshops and status reporting are included • Occasional support for presales activities and for support cases (2nd level)