The Associate Director will provide leadership and operational oversight for clinical trials throughout the development lifecycle, ensuring objectives are met within budget and regulatory standards. They will collaborate cross-functionally to manage CROs, vendors, and study documentation while proactively identifying and mitigating operational risks.
The MSL serves as a field-based scientific expert responsible for engaging with healthcare professionals and supporting clinical development. They translate complex scientific data into clinical insights while ensuring compliant, evidence-based dialogue with thought leaders.
The Clinical Trial Manager will lead the execution of mid- to late-stage global clinical studies from start-up through close-out. They are responsible for coordinating cross-functional teams, overseeing CROs and vendors, and ensuring studies meet quality, budget, and regulatory standards.
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 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 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 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 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 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.
