US Director of Clinical Site Monitoring and Oversight
Amgen · Remote (Remote US)
New this week Posted 2 Nov 2026; checked 7 Nov 2026.
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About the role
Join Amgen’s Mission of Serving Patients
At Amgen, if you feel like you’re part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do.
Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. Amgen is advancing a broad and deep pipeline and portfolio of medicines to treat heart disease, obesity and obesity-related conditions, rare diseases, inflammatory conditions and cancer. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives.
Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
US Director of Clinical Site Monitoring and Oversight
What you will do
Let’s do this. Let’s change the world. In this vital role you will be the strategic leadership and oversight for Amgen’s clinical site monitoring in the US. This role is accountable for defining, implementing, and continuously evolving innovative monitoring strategies that ensure patient safety, data integrity, protocol compliance, and operational excellence. This leader drives strategic transformation of monitoring practices through analytics, technology innovation, and operational excellence while ensuring consistent oversight and inspection readiness across all clinical programs.
Accountabilities
Define and lead Amgen’s US clinical site monitoring strategy, ensuring alignment with corporate quality objectives, regulatory expectations, and industry best practices.
Establish and maintain enterprise standards for on-site, remote, centralized, and risk-based monitoring activities across all clinical programs.
Ensure strategy and execution of field monitoring excellence optimizing central monitoring.
Drive the evolution of monitoring methodologies through the incorporation of advanced analytics, automation, AI-enabled insights, and innovative oversight approaches.
Serve as the monitoring strategy business process owner (BPO) and subject matter expert (SME) for senior leadership, governance committees, inspections, audits, and regulatory interactions.
Collaborate with Clinical Operations leadership to ensure monitoring strategies are integrated into study planning, execution, and oversight models.
Build and oversee a team of internal and FSP clinical research associates (CRAs)
Lead the strategic implementation and continuous enhancement of risk-based monitoring approaches across the portfolio.
Partner with Clinical Risk, Compliance & Systems teams to ensure alignment between monitoring strategies, Critical to Quality (CTQ) factors, Key Risk Indicators (KRIs), Quality Tolerance Limits (QTLs), centralized monitoring and monitoring oversight activities.
Oversee associated procedures and governance of monitoring plans, ensuring monitoring intensity and methodologies are appropriately tailored to study risks.
Drive consistency in monitoring practices.
CRO and Vendor Oversight
Establish a monitoring oversight process to ensure oversight processes proactively identify, escalate, and mitigate emerging quality, compliance, and operational risks.
Provide strategic oversight of CRO monitoring performance, ensuring alignment with Amgen standards, ICH GCP, quality expectations, and contractual obligations.
Continued in Amgen’s original posting ↗.
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