Director

• Lead regional clinical operations strategy aligned with global clinical development goals.
• Ensure monitoring and site management activities meet international regulatory standards, timelines, and budget targets.
• Oversee the quality and consistency of clinical program execution at the site level.
• Build and maintain strategic relationships with service providers and CROs.
• Oversee permanent and functional service provider staff involved in site management.
• Drive continuous improvement in site performance and monitoring practices.
• Identify and mitigate risks to ensure smooth clinical trial execution.
• Collaborate with internal stakeholders across clinical development, regulatory, and data management.
• Ensure alignment between regional execution and global clinical strategy.
• Ensure adherence to GCP, ICH, and applicable regulatory requirements.
• Support audit readiness and inspection preparedness across regional sites.
• Act as the primary point of contact both internally and externally (e.g., vendors) as applicable for anything study related.
• Maintain up to date knowledge of the therapeutic area/product candidate(s), clinical practice, competitors, and regulatory considerations.
• Support audits/inspections and resolutions of findings.
• Support in the development of new SOPs, guidelines etc and/ or participate in working groups about new processes.
• Functional leadership and mentorship of junior staff required; act in advisory capacity to other clinops colleagues within and across TAs.
• When accountable to a set of studies and/or program(s) provides oversight and direction, ensuring appropriate delegation and delivery, inter-program efficiencies and applied learnings.

Associate Director, Site Management, Monitoring Oversight

Associate Director, Global Feasibility Lead

Associate Director, Continuous Improvement Initiatives – Process Management

Senior Director, Site Management and Monitoring Oversight