The Associate Director manages end-to-end operations for nonclinical toxicology and safety pharmacology studies conducted at external CROs. This includes overseeing study forecasting, budgeting, data flow, and ensuring compliance with global regulatory requirements.
The Senior Scientist will lead the analytical pipeline for toxicology studies, including auditing regulatory SEND datasets and creating complex data visualizations. They will also serve as a strategic liaison between internal toxicology teams and project development groups to inform safety strategies and secure governance endorsements.
The Senior Clinical Trial Specialist supports the planning and execution of clinical studies by managing site start-up, tracking study metrics, and coordinating team meetings. They also assist in the oversight of study vendors, maintenance of the Trial Master File (TMF), and data cleaning processes.
The Senior Clinical Trial Manager will lead the end-to-end execution of global clinical studies, ensuring operational strategy, budget adherence, and quality compliance. They are responsible for managing CROs, external vendors, and cross-functional teams to drive study milestones from startup through closeout.
The CMC Technical Writer will review and translate data from CDMOs into scientific reports and regulatory documentation. They will also partner with Quality and Clinical Supply teams to ensure accurate documentation for drug development and submissions.
The Associate Director will serve as a subject-matter expert in neuroscience pharmacology, overseeing the scientific strategy and design of in vitro and ex vivo studies. They will manage external CROs to ensure high-quality data generation and collaborate with cross-functional teams to inform program decisions.
The Senior Director will lead the global medical affairs strategy and execution for the orexin receptor 2 agonist program, focusing on launch readiness and scientific leadership. They will serve as the primary medical voice for the asset, fostering cross-functional collaboration and external engagement with key opinion leaders.
The Director will lead the medicinal chemistry component of a multi-disciplinary CNS drug discovery program, managing internal and CRO-based teams. They are responsible for guiding small-molecule candidates from hit-to-lead through IND-ready status while developing robust intellectual property strategies.
The Manager, Clinical Supply Chain is responsible for the end-to-end planning, execution, and maintenance of clinical supplies across assigned programs. This includes managing demand forecasts, inventory systems, and coordinating with cross-functional teams and external vendors to ensure timely delivery.
The Associate Project Manager provides portfolio-level support by maintaining accurate drug development timelines, budgets, and long-term forecasts within the corporate PPM system. They also assist senior project managers with meeting logistics, status reporting, and monitoring project deliverables.
The MSL serves as a field-based scientific expert responsible for engaging with healthcare professionals and supporting clinical development through evidence-based dialogue. They also collaborate with clinical operations to identify trial sites and provide scientific education to investigators.
The Director will provide strategic leadership for supplier quality management, including managing GxP audit programs and driving global inspection readiness. They will also collaborate with cross-functional teams to oversee supplier performance and ensure the robustness of quality systems.
The Inventory Control Manager will oversee inventory planning, control, and reconciliation for clinical supply materials across an outsourced network. They will partner with internal teams and external vendors to ensure real-time visibility, prevent stockouts, and minimize waste.
The Director will provide leadership for analytical quality control, stability programs, and specification management across clinical and commercial development. They will also oversee supplier relationships and provide tactical support for regulatory submissions and health authority inspections.
