Clinical Trials Manager

Role Overview

• Coordinating and supervising all aspects of a clinical study
• Monitors clinical trial sites
• Assists Clinical Program Manager in overall study management
• Drafts and coordinates review of relevant documents
• Maintains study timelines
• Contributes to development of study budget
• Manage CROs/vendors
• Ensures effectiveness of site budget/contract process

Requirements

• Bachelor's Degree and 5 Years' Experience OR Masters' Degree and 3 Years' Experience
• 6+ years of experience and an RN (2 or 3 year certificate)

Benefits

• Discretionary annual bonus
• Discretionary stock-based long-term incentives
• Paid time off
• Company-sponsored medical insurance
• Company-sponsored dental insurance
• Company-sponsored vision insurance
• Company-sponsored life insurance plans