Imagine how your ideas and expertise can change a patient’s life. We generate extensive clinical evidence to demonstrate the effectiveness and safety of our innovations and how our products transform patients’ lives. As part of our Clinical Affairs team, you’ll hone your scientific curiosity and passion for evaluating data to increase access to pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize patient outcomes. **How you'll make an impact:** **Professional Education – Proctor Governance & Logistics** + Lead projects focused on **Proctor Governance** . + Ensure **accurate and complete documentation** of proctor training and certification. + Oversee the **end-to-end logistics** of proctor participation in procedures: + Build and maintain a **Proctor Logistics Dashboard** , ensuring data accuracy and visibility. + Manage proctor travel arrangements and maintain full documentation aligned with internal compliance standards. + Develop a solid understanding of the **product portfolio** and **clinical procedures** . **    2. Clinical Research Support** + Provide operational support for **clinical research activities** + Track and follow up on **milestones for all active clinical studies** , ensuring proper progress and payment execution. + Manage approval workflows, maintain documentation, and support **back-office operations** for multiple ongoing studies. + Follow up with **Ethics Committees** on protocol approvals and required submissions. + Support **site visits** , including coordination for Advanced Technologies (Outflow) studies. **What you'll need** + Understanding of **clinical procedure workflows** . + Bachelor’s degree in a **health-related field** (e.g., Biomedical Engineering, Biomedicine, Nursing, or related). + Previous **corporate experience** . + Foundational understanding of **clinical research** . + **Intermediate English** (reading and writing). + Strong soft skills: + Organization + Teamwork + Clear communication **What else will help you:** + Demonstrated problem-solving and critical thinking skills + Proven expertise in MS Office Suite, including Word, Excel, Adobe, and ability to operate general computer software and office machinery + Strong understanding of cardiovascular anatomy, pathology and physiology or Business Unit area of expertise + Understanding of medical device regulatory requirements and documents, device accountability and adverse events reporting + Technical writing skills (protocols, CRF development, study tools) + Ability to communicate and relate well with key opinion leaders and clinical personnel + Experience in training new hires + Adhere to all company rules and requirements (e.g., pandemic protocols, Environmental Health & Safety rules) and take adequate control measures in preventing injuries to themselves and others as well as to the protection of environment and prevention of pollution under their span of influence/control