Clinical Development
Clinical Evaluation Associate
Opportunity summary
Do you enjoy working with scientific data while navigating complex regulatory requirements? Are you motivated by reviewing literature and transforming insights into clear, high-quality documentation? And are you curious about—or already experienced in—the medical device industry? If so, this could be your next step.
The role
As a Clinical Evaluation Associate at Ambu, you will be responsible for creating, maintaining, and updating clinical evaluations for Class I and II medical devices in accordance with MDR (EU) 2017/745. You will work closely with experienced colleagues and gradually take on more responsibility as you develop in the role.
When involved in innovation projects, you will be part of the R&D core team, contributing from early clinical strategy through to planning, execution, and reporting.
Key responsibilities
In this role, you will:
Author and maintain high-quality clinical evaluation documentation in line with regulatory requirements, applying a structured and analytical approach Conduct systematic literature reviews to collect and assess clinical data supporting device safety and performance Identify evidence gaps a1 …
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