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.
The Senior Medical Director will provide strategic leadership for clinical development programs in dermatology, overseeing study design, execution, and regulatory submissions. They will collaborate with cross-functional teams to ensure safety, data integrity, and successful advancement of the antibody portfolio.
