The Executive Director will provide strategic leadership and hands-on oversight of global clinical trials, ensuring they are delivered within timelines and budgets while meeting quality standards. They will lead trial execution from start-up through close-out, managing CROs, vendors, and cross-functional teams to achieve corporate development objectives.
The Senior Scientist will manage outsourced bioanalytical and biomarker activities at CROs, including assay development, validation, and sample analysis. They will also serve as the primary scientific point of contact to ensure data quality and adherence to regulatory requirements.
The Director, Drug Safety Physician will lead medical review of Individual Case Safety Reports and oversee aggregate safety monitoring and signal detection activities. They will also provide medical safety strategy for clinical trials and ensure compliance with global regulatory requirements.
The Senior Director will provide operational leadership for pharmacovigilance activities, including case management, vendor governance, and regulatory compliance. They will also oversee safety database operations, inspection readiness, and the management of safety management plans and vendor oversight.
The Associate Director will independently lead end-to-end clinical supply chain operations for global studies, including demand planning, distribution, and inventory management. They will collaborate with cross-functional teams and external partners to ensure compliant, cost-effective, and uninterrupted supply of clinical materials.
