Clinglobal Group

The specialist will lead the scheduling and coordination of third-party qualification audits and oversee CAPA progression and site deviations. They will also serve as the primary QA liaison for global SOP reviews and computerized system validation documents.

Coordinate all phases of Field Clinical Trials, managing resources, timelines, and budgets to ensure quality completion. Serve as the primary contact for sponsors and oversee communication between internal teams and external partners.

The QA Process and System Specialist will lead third-party audit coordination and oversee CAPA progression and site deviations. They will also serve as the primary liaison for SOP reviews and support computerized system validation and change management.

The Clinical Project Manager will oversee and manage clinical projects to ensure they are delivered within timelines, budgets, and quality standards while adhering to regulatory guidelines. They will serve as the primary liaison for sponsors and coordinate cross-functional teams to align project objectives.

The Study Monitor is responsible for performing monitoring activities to ensure clinical trials adhere to study protocols, VICH GL9 GCP guidelines, and regulatory requirements. This includes verifying data accuracy, maintaining site adherence to quality standards and timelines, and serving as a primary contact for assigned study sites.

The Clinical Project Manager will oversee and actively engage in monitoring and clinical project management activities, ensuring studies adhere to scientific designs, timelines, and regulatory guidelines like VICH GL9 GCP. This role involves serving as the Sponsor's primary liaison, providing strategic leadership in the planning, execution, and delivery of clinical projects in animal health research.