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Strong fit if you have site monitoring leadership, quality oversight, and client-facing FSP discipline—and want CRO trial delivery rather than pure bedside care.
As Clinical Site and Monitoring Health Lead (US FSP) at Parexel, a typical day centers on FSP-client site health: review monitoring metrics and risk signals, coach CRAs/site teams, escalate quality or enrollment issues, align with sponsor SOPs, and document corrective actions so trial delivery stays inspection-ready.
Build deep ICH-GCP, risk-based monitoring, CAPA, and FSP client communication. Free upskilling: Saylor Academy — Health Sciences courses (free); Coursera — audit-track healthcare courses (free to learn).
Data marks remote as off; expect work tied to the Frankfort, KY listing and U.S. site oversight patterns.
Functional Service Provider: you typically embed with a sponsor’s model while employed by Parexel for monitoring/site-health delivery.
Parexel is a long-standing CRO focused on running trials for pharma/biotech—site quality and timeline reliability are core.
Website: parexel.com
Parexel is an American contract research organization. It conducts clinical trials on behalf of its pharmaceutical and biotechnology clients to expedite drug development and clinical trial progress.
Public cache only — not an employee review.
Parexel is hiring a Clinical Site and Monitoring Health Lead (SMH Lead) to work in Frankfort, Franklin County. In this full-time, site-facing role, you'll apply your expertise in clinical trial regulations and monitoring to safeguard trial quality and ensure effective CRO oversight at investigator sites. About the Role The Clinical Site and Monitoring Health Lead plays a critical role in ensuring clinical trials are executed with integrity. You'll combine deep knowledge of Good Clinical Practices (GCPs) and regulatory requirements with hands-on monitoring experience to assess trial conduct at investigator sites. Working directly in the field, you'll ensure that clients have full visibility and confidence in the quality of their trials. What You'll Do Leverage monitoring expertise to evaluate and safeguard the quality of clinical trial execution at investigator sites Apply knowledge of clinical trial regulations and GCPs to assess regulatory compliance and operational readiness Oversee site-level activities that protect trial integrity, data quality, and participant safety Ensure the client can effectively oversee CRO monitoring performance and impact Identify risks, document findings, and recommend corrective actions to enhance trial conduct Maintain regular communication with site teams and stakeholders on monitoring activities and outcomes What We're Looking For Solid knowledge of clinical trial regulations and Good Clinical Practices Hands-on experience in clinical monitoring and site oversight roles Understanding of contract research organization (CRO) operations and client relationships Strong communication and interpersonal skills to work effectively across diverse teams Ability to work independently while maintaining high standards for trial quality Current residence within 1 hour of an international airport How to Apply To apply for this Clinical Site and Monitoring Health Lead position at Parexel, submit your application through this listing.
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