Associate Director, Clinical Study Lead

Role: Senior-level Clinical Study Lead responsible for operational oversight of global clinical studies within specified regions, ensuring timely, compliant, and quality-driven delivery. Responsibilities include study planning, start-up, execution, vendor management, monitoring, risk mitigation, and study close-out, with a focus on cross-functional coordination, regulatory compliance, and vendor oversight. Qualifications: Bachelor's degree in life sciences or related field; 7+ years in pharma, biotech, or CRO with at least 6 years in clinical research, including Phase 1-3 studies management. Experience managing outsourced models, CRO oversight, and regulatory compliance (ICH-GCP, FDA, EMA) essential. Skills: Strong project management, risk assessment, global cross-cultural communication, and problem-solving capabilities. High-Value: Experience leading regional/global studies, managing CRO/vendor relationships, working within regulated environments, and traveling domestically and internationally. WorkSetup: Not specified, but involvement in global studies implies flexible, possibly hybrid or remote work with travel.