The Global Project Manager leads cross-functional clinical projects, ensuring they meet time, cost, and quality goals from protocol concept to final report. They serve as the primary operational contact for clients, managing budgets, regulatory compliance, and site performance across global regions.
The Vice President of Quality Assurance is responsible for implementing and maintaining quality system processes to ensure compliance with cGCP and governmental regulations. They provide leadership for regulatory strategy, oversee internal and external audits, and manage the development of the quality and regulatory department.
The Study Start-up Lead oversees the full lifecycle of regulatory submissions for global clinical trials, ensuring all startup deliverables are met within scope and compliance. This role provides strategic leadership, cross-functional coordination, and subject matter expertise to support SSU specialists and investigative sites.
