Job Description

Are you a clinical operations pro ready to make your mark at a fast-growing, cutting-edge research network? We’re on the hunt for a Clinical Research Site Manager to join a dynamic, forward-thinking clinical trial site leading the charge in innovative health research.

In this pivotal role, you’ll oversee high-impact studies from startup to closeout, guiding teams and managing every detail to ensure world-class execution. If you thrive in a fast-paced environment and want to directly shape the future of clinical trials, this is your moment.

What You’ll Do:

• Lead and mentor a high-performing clinical study team
• Coordinate all trial activities—start-up, vendor management, patient visits, regulatory compliance
• Ensure GCP, FDA, ICH, and HIPAA compliance across every touchpoint
• Roll up your sleeves in screening, consenting, data entry, and lab procedures
• Collaborate closely with site leaders and investigators to deliver seamless operations
• Help drive continuous process improvements and quality initiatives

What You Bring:

• Proven experience managing clinical trials (site-level experience preferred)
• Strong knowledge of GCP, ICH, and FDA regulations
• Hands-on approach to leadership and study coordination
• Passion for improving patient outcomes through research
• Be part of something bold. Join a team where your expertise matters—and where your impact will be felt every day.

Apply now to step into a role where clinical excellence meets meaningful purpose.

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