Associate Director, Clinical Science

Role: Associate Director (AD), Clinical Science in global clinical development, collaborating with medical, statistical, safety, and pharmacology teams to support investigational drug development. Responsibilities: contribute to study design, protocol development, regulatory document preparation, clinical data review, safety monitoring, risk management, investigator engagement, and regulatory interactions; ensure compliance and quality of clinical documentation; support audits and inspections; participate in trial reporting and publications. Requirements: college degree in life sciences or nursing; advanced degree preferred (PhD, PharmD, MS); 8+ years in pharma/biotech, with experience in complex cardiovascular trials, proof of concept, pivotal studies, and regulatory filings; skills in scientific analysis, cross-functional teamwork, investigator relationship management, and team leadership in matrix settings. HighValue: cardiovascular therapeutic area, complex proof-of-concept and pivotal trials, regulatory submissions including NDAs, clinical safety and data review, documentation, and compliance. WorkSetup: not specified; emphasis on multinational team collaboration.