Oversee and actively engage in monitoring and clinical project management activities to ensure studies are conducted in adherence to scientific designs, timelines, and regulatory guidelines (e.g., VICH GL9 GCP)
Serve as the Sponsor's primary liaison, fostering effective communication and providing updates to the study team members and management
Responsible for providing strategic leadership and oversight in the planning, execution, and delivery of clinical projects
Plan, coordinate, and manage clinical projects to ensure delivery within timelines, budgets, and quality standards while adhering to regulatory guidelines
Collaborate with cross-functional teams to align project activities and objectives
Develop and maintain project documentation
Identify and address risks or challenges impacting project timelines, quality, or budgets, and implement corrective actions as needed
Coordinate human and material project resources and ensure availability to meet project milestones and deliverables

DVM or related Life Sciences degree
Minimum of three years of experience in Field Clinical Trials and Project Management
Familiarity with regulatory guidelines such as VICH GL9 GCP and their application in clinical trial management
Strong organizational skills to effectively manage clinical projects, ensuring delivery within timelines, budgets, and quality standards
Ability to work and communicate in English
Solid understanding of clinical project management processes, including planning, coordination, and execution

Clinglobal

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