Associate Director, Clinical Trial Disclosure & Transparency

Role: Associate Director specializing in Clinical Trial Disclosure and Transparency, leading global strategy and operational execution to ensure compliant, timely disclosure of clinical trial information across regions and study types. Responsibilities: oversee registration, results disclosure, and lay summaries; guide regional teams and CROs; support transparency activities such as anonymization; collaborate with cross-functional stakeholders (Clinical Development, Medical Affairs, Regulatory, Legal, Data Privacy); manage vendor relationships; monitor and report compliance metrics; influence industry standards and regulations (FDA, EMA, UK MHRA, Health Canada). Requirements: 10+ years in pharma/biotech with deep drug development knowledge; strong regulatory interpretation skills; proven experience managing global disclosure projects; excellent communication, influencing, and critical thinking abilities; familiarity with ICH-GCP, GDPR, industry standards; hands-on with disclosure systems (e.g., Trialscope). Preferred: experience in biopharma with a focus on regulatory compliance and transparency, working knowledge of international disclosure regulations. Work setup: in-office 3 days/week.