Quality

• Supports the identification of operational risks and issues and works with the Global Clinical Study Manager to recommend solutions for discussion with appropriate team leadership
• Learns and shares best practices in clinical operations methodologies, systems and processes with an emphasis on quality and compliance
• Suggest improvements to enhance efficiency and the quality of the work performed on assigned projects
• Might support the development of global study tools, working instructions and SOPs
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Budget

• Supports selection and set-up of vendors for global outsourced activities
• Supports study budget management activities with responsibility for PO setup and payment invoice tracking across all study lifecycles.
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Supervisory Responsibilities

Might mentor junior team members/onboarding of new hires

Qualification Required

Education Required: Bachelor or higher degree in a scientific or healthcare discipline*, higher degree preferred.

Computer Skills

Proficiency in MS Office Suite, including Excel, PowerPoint, and Project etc.

Other Qualifications

• Knowledge of clinical operations methodologies, understanding of operational aspects of clinical study processes
• 3 or more years of experience in clinical research within Biotech, Pharma or CRO industry
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