General Manager, Clinical Trials and Site Management

Location: Brentwood, TN. (Onsite Preferred; Remote Considered)

IVX Health is a national leader in high‑quality infusion and injection therapy, operating 150+ ambulatory centers across the U.S. Backed by Linden Capital Partners, we continue to scale rapidly—expanding services, accelerating growth, and building the leading ambulatory infusion platform in the country.

We are launching a clinical trials platform across our national footprint and seeking a senior operator to build, lead, and scale this new business.

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About the Role

The General Manager, Clinical Trials & Site Management will design and run IVX Health’s clinical trials operating model - from start-up through national expansion. This leader will ensure compliant, inspection‑ready performance across all sites, serve as the external-facing executive for sponsors and CROs, and ultimately own the P&L for the clinical trials service line.

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What You’ll Do

• Build and operationalize a scalable clinical trial site management model leveraging IVX Health’s clinical and operational infrastructure.
• Lead execution of clinical trials across multiple sites, ensuring protocol adherence, predictable study start‑up, and high‑quality administration and documentation.
• Serve as the senior accountable leader for regulatory compliance, quality, SOP governance, training, documentation integrity, and CAPA.
• Partner with Clinical, Operations, Legal, Finance, and Regional teams to integrate research into daily clinical workflows.
• Represent IVX Health as an operational subject matter expert in sponsor and CRO discussions, supporting feasibility, execution, and compliance credibility.
• Build and lead a centralized trials team to support scale and standardization.
• Assume increasing financial accountability, evolving to full P&L ownership and long‑term strategic planning.

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What You Bring

Required

• 10+ years of senior experience in clinical trial site management, SMO leadership, or research operations within an academic medical center.
• Direct, hands-on leadership of clinical trial sites and active studies from start‑up through close‑out.
• Deep expertise in FDA regulations, ICH GCP, IRB requirements, inspections, audits, and CAPA management.
• Proven ability to lead cross‑functional teams and serve as a credible executive with sponsors and CROs.

Preferred

• Experience executing or scaling multi‑site clinical trials.
• Exposure to P&L ownership or financial accountability (formal GM title not required).
• Background in infusion-based or procedure-intensive trials.
• Experience scaling operations while maintaining high regulatory and quality standards.