Prague, CZE
1 day ago
Associate Specialist, Clinical Compliance
Innovation starts from the heart. Edwards Lifesciences is the leading global structural heart innovation company, driven by a passion to improve patient lives. With millions of patients served in over 100 countries, each team makes a meaningful contribution by improving patient outcomes and discovering lasting solutions for unmet patient needs. Our Associate Specialist, Clinical Compliance position is a unique career opportunity that could be your next step towards an exciting future. **How you’ll make an impact:** + Collaborate with clinical teams to maintain compliance and address non-compliance issues. + Manage the learning management system, training plans, and study rosters; identify and resolve training gaps. + Conduct compliance assessments and recommend solutions for low-impact regulatory and procedural gaps. + Support internal and external audits, including preparation, team coordination, and follow-up. + Partner with Clinical Affairs teams to resolve low-impact issues and improve processes. + Analyze trends and metrics to identify and address non-compliance and enhance operational efficiency. + Review audit findings and ensure timely resolution with responsible parties. + Develop and deliver training materials on regulatory updates, best practices, and procedural changes. + Perform other related duties as needed. **What you'll need (Required):** + University degree and some years of relevant work experience e.g. clinical trials, clinical compliance, clinical monitoring, regulatory compliance or quality assurance/control etc. + Full proficiency in English, other language is a plus. **What else we look for (Preferred):** + High attention to detail, solid problem-solving, organizational, and analytical abilities + Strong computer skills with the ability to efficiently use various software tools and adapt to new technologies quickly. + Working knowledge of clinical compliance policies and procedures + Familiarity with medical device regulations (e.g., FDA, ISO 14155/13485, ICH) + Ability to stay current on clinical laws, regulations, and standards
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