Associate Director of Clinical Operations

Job Summary

Leading the execution of clinical trials across all phases, the full-time Associate Director of Clinical Operations will manage day-to-day trial activities, oversee site activation and enrollment, and ensure high-quality data delivery while working remotely.

Key responsibilities

• Lead day-to-day clinical trial execution for assigned studies, including site activation, enrollment, monitoring, and closeout activities
• Serve as the primary clinical operations lead, acting as the main point of contact for CROs, vendors, and clinical sites
• Provide direction and mentorship to Clinical Trial Managers, ensuring consistent quality of study execution across the team

Required qualifications

• Bachelor's degree in life sciences or a related field
• Minimum 8-10 years of experience in Clinical Operations within the biopharma industry, including global trial experience
• Demonstrated ability to independently lead clinical trials from start-up through close-out
• Strong understanding of CRO/vendor oversight and clinical development processes
• Experience in maintaining a submission-ready eTMF and knowledge of ICH-GCP and global regulatory requirements