Job Summary

• The role involves leading or supporting the clinical protocol development process and serving as the responsible author for clinical protocols.
• Candidates must demonstrate the capability to interpret, discuss, and represent trial-level data while managing multiple clinical trials concurrently.
• The position requires a track record of successfully managing study budgets and collaborating with key partners to set vendor strategies.

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Skills & Requirements

Key Requirements

• Bachelor's degree in life science/healthcare required
• 6+ years experience in clinical trials/development
• Proficient in early clinical development methodology
• Working knowledge of clinical finance principles

Work Rights