Senior Global Trial Associate

Contributes to the operational execution of clinical studies to ensure delivery on time, within budget, and of high quality in compliance with ICH/GCP, Regulatory Authorities' regulations/guidelines, and applicable SOPs/WPs.

Requirements

• Knowledge of ICH/GCP, regulatory guidelines and directives, and the drug development process.
• Knowledge of clinical research budgets including processing and tracking of site and vendor payments is preferred.
• Working knowledge of project management preferred.
• BA/BS in relevant discipline strongly preferred.
• Minimum 2-4 years' experience in Clinical Research or related work experience. Global experience is preferred.

Benefits

• Competitive salary
• Benefits package
• Flexible work arrangements
• Opportunities for career growth and development