Associate Director, Clinical Operations

Role

Associate Director, Clinical Operations leading global oncology Phase 2/3 trials, including NSCLC and CRC indications, with a focus on operational execution and vendor management.

Responsibilities

• oversee clinical trial planning
• ensuring compliance with GCP/ICH
• manage CROs and external vendors
• mitigate operational risks
• control budgets
• maintain inspection readiness
• foster cross-functional collaboration across Regulatory, Clinical Science, Data Management, and Quality teams
• Lead the development and approval of study plans
• manage TMF quality
• drive process improvements

Qualifications

• Bachelor's degree in life sciences or related field; 10+ years of experience managing international oncology clinical trials, with strong leadership, regulatory, and operational expertise.

Preferred

• deep knowledge of drug development, GCP/ICH, and complex global study execution.

High-Value

• Oncology (NSCLC, CRC), Phase 2/3, international, vendor oversight, inspection readiness, cross-functional leadership.

Work Setup

not specified; travel up to 20%.