The Senior Clinical Project Manager will lead complex clinical trials from start-up to close-out, ensuring all project milestones are met within scope, budget, and timeline. They will act as the primary point of contact for sponsors while managing multidisciplinary teams and driving compliance with regulatory standards.
The Senior Clinical Research Associate will independently manage monitoring activities, including site selection, initiation, and close-out visits to ensure protocol compliance and data integrity. They will also proactively identify and manage study risks, maintain strong relationships with site teams, and support inspection readiness.
The role involves generating and qualifying new business opportunities through targeted outreach to biotech and pharmaceutical prospects. You will manage prospecting activities within the CRM and partner with Business Development to advance opportunities toward RFPs.
The Director of Study Operations will provide strategic leadership and end-to-end accountability for the performance, quality, and budget of the Study Operations function across North America. This role involves managing regional teams, overseeing resource planning, and representing the department in cross-functional forums and client interactions.
Lead complex, global cardiometabolic clinical trials from start-up to close-out while ensuring adherence to scope, budget, and timelines. Manage multidisciplinary teams and act as the primary point of contact for sponsors to drive project excellence and regulatory compliance.
The Expert Modeller provides high-level statistical advice for epidemiological studies and manages complex analytical processes for specific projects. They are responsible for supervising other statisticians, designing advanced methodologies, and acting as the primary point of contact for modelling queries.
