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The Project Lead manages clinical trials, ensuring adherence to contracts, optimizing study performance, and leading cross-functional project teams while working with stakeholders to enhance operational excellence.

The Scientist - ADME performs laboratory assays, executes analytical procedures, supports method development, troubleshoots equipment, and ensures data compliance.

The Contracts Manager will draft, review, and negotiate contracts, manage legal reviews, and communicate with stakeholders to ensure efficient contracting processes.

As a Study Start-Up Clinical Research Associate, the role involves site selection, start-up activities, document preparation, and ensuring timelines and compliance in Phase I-IV trials.

As a Key Account Manager, you will promote pharmaceutical products, build customer relationships, and improve patient outcomes through your sales expertise.

The Associate Director of Supplier Services leads the Hospital Pharmacy Analytics strategy, managing supplier relationships and ensuring compliance with NHS data governance.

The Site Activation Specialist manages clinical trial start-up processes, including feasibility, site identification, and regulatory submissions, while ensuring compliance with regulations.

The Project Management Analyst supports clinical trial delivery by coordinating project schedules, managing project finances, and ensuring timely communication. Responsibilities include dashboard management, risk tracking, project reporting, and supporting the onboarding of new team members. They liaise closely with the Project Leader and clinical teams to enhance operational effectiveness and compliance.

The role involves managing programming staff, developing statistical procedures, and executing programming for health data studies, particularly involving Swedish datasets.

The Clinical Research Associate performs site monitoring visits, manages study progress, ensures compliance with regulations, and maintains documentation related to site management and monitoring.