A company is looking for a Director of Clinical Evaluation and Excellence.Key ResponsibilitiesLead clinical development strategies to align with corporate and regulatory goalsOversee design, execution, and reporting of clinical trials and ensure compliance with global regulatory standardsManage a team of regulatory specialists and ensure high-quality documentation for regulatory submissionsRequired QualificationsBachelor's degree in Life Sciences or related field (advanced degree preferred)Minimum 10 years of experience in clinical research, regulatory affairs, and quality assurance within the medical device industryProven leadership in global regulatory strategy and clinical documentationStrong understanding of FDA, EU MDR, ISO 13485, ISO 14155, and ICH GCP regulationsRAC certification preferred