The Associate Director of Clinical Operations will have program-level accountability for clinical trials timelines, budgets, quality, and ensuring compliance with Good Clinical Practice (GCP) and may mentor and manage Clinical Trial Managers and other clinical operational staff in the execution of clinical trials.

This role works closely with Medical Monitors, cross-functional representatives, CROs, and other study vendors to ensure successful completion of all clinical study activities and project deliverables within the required time frame and budget.

Responsibilities

• Partner with Clinical Operations leaders on strategy for successful implementation and execution of clinical trials
• Ensure trials are carried out according to the study protocol, SOPs, and ICH/GCP guidelines/regulations and study specific manuals and procedures
• Independently and strategically develop and manage the trial’s timelines, study budget, key deliverable...