Associate Director Site Management & Oversight Lead - Remote

Overview

The Associate Director Site Management & Oversight Lead is responsible for the strategic and operational oversight of clinical trial site management and monitoring activities to ensure high quality and compliance.

In Short

• Accountable for oversight of investigational site activities across clinical studies.
• Ensures compliance with regulatory standards and quality in clinical trials.
• Partners with internal and external stakeholders for effective study oversight.
• Identifies and mitigates risks impacting recruitment and data quality.
• Maintains strong relationships with investigators and site staff.
• Supports audit and inspection planning and implementation.
• Provides study support on escalated site issues.
• Collects feedback to advocate for process improvements.
• Contributes local site intelligence for feasibility teams.
• Oversees vendors and CROs effectively.

Requirements

• Bachelor’s degree in life sciences or related field.
• 12+ years of clinical research experience in the pharmaceutical industry.
• Experience in managing large and complex global clinical trials.
• Thorough knowledge of ICH guidelines and GCP.
• Strong budget forecasting and management skills.
• Ability to mentor and coach team members.
• Excellent understanding of the clinical development process.
• Skilled in navigating clinical project challenges.

Benefits

• Comprehensive health and wellness programs.
• Support for professional development and career growth.
• Diverse and inclusive workplace culture.
• Flexible work arrangements.
• Opportunities to work on innovative therapies.