Job Summary

• Lead or support the clinical protocol development process in collaboration with the Medical Lead and other line functions, acting as the responsible author for clinical protocols and amendments.
• Lead or support a global cross functional CTT to ensure all trial deliverables are met, setting stretch goals and presenting actionable alternatives to accelerate timelines.
• Responsible and accountable for forecasting and managing overall study budget(s) in collaboration with key partners, and implementing best practices for trial management.

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Skills & Requirements

Key Requirements

• Bachelors in life science/healthcare
• Approximately 6+ years experience
• Proficient in early clinical development
• Operational project management experience
• Track record managing multiple trials
• Working knowledge of clinical finance

Work Rights