At Chiron Consulting, we specialize in driving operational excellence across clinical development and regulatory strategy for small to mid-sized biopharma and CRO organizations. With deep experience in a variety of therapeutic areas, we provide hands-on leadership and tailored solutions that accelerate timelines, optimize resources, and ensure inspection-ready quality at every stage.

Our core capabilities:
• Full-Scope Clinical Trial Management (Phases I–IV): Experience designing and operationalizing trials from proof of concept through commercial launch.
• Therapeutic Experience with Focus: Broad exposure including neurology, infectious disease, oncology, cardiovascular, and metabolic disorders—with particular expertise in rare disease and pediatric populations.
• Quality-First Operational Leadership: Emphasis on GCP compliance, audit/inspection readiness, and building quality systems that scale. 
• Legal Acumen in Clinical Context: A JD background providing a unique edge in navigating complex contracts, data privacy considerations, and compliance frameworks.
• Global Trial Execution: Proven ability to manage programs across North America, EU, APAC, and Latin America.
• Team Building & Cross-Functional Leadership: Strong record of growing clinical operations teams and leading collaboration across clinical development, medical affairs, regulatory, and commercial functions.

Founded by a seasoned Clinical Operations executive with a background in law and science, Chiron brings pragmatic, cross-functional insight to every engagement. Whether you're preparing for first-in-human studies, scaling your clinical infrastructure, or navigating global trial execution, Chiron delivers the clarity and execution support needed to move forward with confidence.
Let’s build smarter, faster, and better together.

Biotechnology

Clinical Trials

Chiron Consulting LLC

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