Principal Global Trial Associate

Provides operational support for global insourced or outsourced clinical trials from concept to final clinical study report. May be responsible for managing country planning, protocol level attributes and milestones/drivers in CTMS.

Requirements

• Bachelor's degree in relevant discipline
• 4-6 years of clinical research/global study operations experience
• Knowledge of ICH/GCP, regulatory guidelines/directives, drug development, and clinical research processes

Benefits

• Competitive salary
• Additional incentive cash and stock opportunities
• Life insurance
• Health insurance
• Retirement plan
• Paid time off