Clinical & Regulatory Affairs

Anteris Technologies is a worldwide leader in structural‑heart innovation, dedicated to transforming cardiac care through science‑driven products. The company's flagship project, the DurAVR THV valve, incorporates proprietary ADAPT® anti‑calcification technology to emulate the natural motion of a healthy heart valve. The Clinical & Regulatory Affairs function supports the entire lifecycle of these breakthrough devices, from early research to market launch. In this position you will be involved in a variety of daily tasks that keep clinical programmes moving forward. Core duties include managing clinical operations, performing site monitoring, providing direct support to physicians, delivering field‑based clinical education, and ensuring adherence to global regulatory standards. You may also oversee the planning and execution of clinical trials specific to medical‑device products, coordinating activities across multiple regions and functional teams. The employer seeks candidates who already possess hands‑on experience in several key areas. Proven background in clinical operations, clinical monitoring, physician support, and field clinical education is essential. Candidates must also have demonstrated ability to maintain global regulatory compliance and to manage clinical trials within the medical‑device sector. Experience with Class III devices, structural‑heart therapies, cardiovascular technologies, or worldwide clinical studies is viewed as highly valuable. The ideal applicant works well in collaborative, adaptable, and organized ways, thriving in fast‑paced, cross‑functional environments. Anteris offers a competitive remuneration package that includes salary, performance bonuses, and equity participation, together with a broad suite of health and wellness benefits. The work setting is described as collaborative and dynamic, fostering a culture of innovation and excellence. Employees benefit from career‑development programmes and the chance to contribute to therapies that impact patients globally. The company emphasizes an inclusive environment and may request proof of COVID‑19 vaccination to meet regulatory and travel requirements. What the role asks for: - Experience in clinical operations - Experience in clinical monitoring - Experience in physician support - Experience in field clinical education - Experience in global regulatory compliance - Experience in clinical trial management - Experience with Class III medical devices - Experience with structural‑heart therapies - Experience with cardiovascular technologies - Experience with global clinical studies - Collaborative mindset - Adaptable work style - Organized approach - Ability to work in fast‑paced environments - Proof of COVID‑19 vaccination (if required)