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