Principal Scientist - Clinical Trials Manager

Key Responsibilities

• Aid Efficacy Leads in designing clinical studies
• Prepare and review clinical study protocols with Efficacy Leads and Biostatistician
• Collaborate with Study Monitors for clinical site selection, qualification, and training
• Select and coordinate central laboratories and external vendors
• Work with Clinical Data Managers to establish robust Electronic Data Capture databases
• Create and approve clinical study budgets and invoices

Key Performance Indicators

• Meet project timelines and enrollment targets
• Evidence of excellent data integrity and quality through audits and FDA reviews