Site Director

Benefits

Qualifications

• •5+ years of clinical research site experience, with a strong foundation as a CRC
• •Demonstrated ability to manage studies end-to-end, including enrollment and execution
• •Prior experience leading, mentoring, or developing team members
• •Strong knowledge of GCP, FDA regulations, and clinical trial operations
• •Experience working with sponsors and CROs
• •Proven ability to manage competing priorities in a fast-paced environment
• •Strong business mindset with exposure to site metrics, budgets, or performance goals
• •Drive real impact – Influence patient access to clinical trials and site-level success
• •5 more items(s)

Responsibilities

• •Whether you’re a Senior/Lead CRC looking to step into site leadership or a current Site Manager ready for broader ownership, this is an opportunity to take full responsibility for site performance, team development, and clinical trial execution
• •As Site Director, you’ll move beyond day-to-day coordination to lead the strategy, operations, and growth of a clinical research site—while still leveraging the deep operational expertise you built as a CRC
• •Lead the overall operational and financial performance of the clinical research site, including study execution, enrollment, and profitability
• •Oversee all active clinical trials to ensure compliance with protocols, GCP, FDA regulations, and internal SOPs
• •Monitor key performance metrics (e.g., enrollment, timelines, data quality) and implement improvements to drive site success
• •Manage, coach, and develop a team of CRCs, research assistants, and site staff, fostering a high-performance and patient-focused culture
• •Support hiring, onboarding, and ongoing performance management of site personnel
• •Partner with internal teams to develop and execute patient recruitment strategies; monitor and optimize enrollment performance
• •Build and maintain strong relationships with sponsors and CROs, ensuring high-quality delivery and repeat business
• •Manage site budgets, staffing models, and resource allocation to optimize efficiency and financial outcomes
• •Ensure audit readiness at all times; lead responses to audits, inspections, and quality findings
• •Oversee regulatory documentation, source quality, and data integrity across all studies
• •Identify operational challenges and implement scalable solutions to improve site performance
• •Expand your scope – Move from managing studies to leading an entire site
• •Lead with credibility – Your CRC experience will directly shape how you coach and develop your team
• •12 more items(s)