Study Delivery Senior Manager – Study Delivery Lead

Amgen

. Own end-to-end delivery of assigned global clinical studies, with accountability for quality, timelines, budget, and operational performance .

Posted 10/9/2026full-timeRemote • United StatesSenior💰 $163,721 - $197,116 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in managing global clinical studies with a focus on quality, timelines, and budget management. Proven ability to lead cross-functional teams, ensure regulatory compliance, and drive continuous improvement in clinical trial delivery.

Highest-signal resume keywords

Clinical Execution ExperienceGlobal Clinical Trials ManagementRegulatory Audit RepresentationCross-Functional Team LeadershipVendor Oversight

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Study DesignRisk ManagementData Integrity AssuranceFeasibility AssessmentSite SelectionParticipant RecruitmentData MonitoringCorrective Action ImplementationQuality-By-Design ApproachesBudget Management

Soft Skills

LeadershipCollaborationProblem-SolvingCommunicationStakeholder Engagement

Industry Keywords

BiopharmaceuticalClinical Research Organization (CRO)Life SciencesClinical Trial DeliveryRegulatory ComplianceVendor ManagementEnrollment StrategiesOperational PerformanceContinuous ImprovementEvidence Generation Strategy

About the role

Key responsibilities & impact

Own end-to-end delivery of assigned global clinical studies, with accountability for quality, timelines, budget, and operational performance
Lead and align cross-functional study teams to deliver high-quality clinical data in line with the evidence generation strategy
Define and implement study plans covering feasibility, site selection, site engagement, recruitment and retention, and vendor delivery
Identify and manage study risks using quality-by-design and risk-based approaches to ensure participant safety and data integrity
Oversee global study execution, including enrollment, data flow, monitoring, and corrective actions
Provide leadership, direction, and escalation management to resolve complex study issues across geographies
Build partnerships with internal stakeholders and external vendors to ensure effective collaboration and performance
Champion continuous improvement, innovation, and regulatory compliance throughout clinical trial delivery

Requirements

What you’ll need

Doctorate degree and 2 years of Clinical Execution experience, or Master’s degree and 4 years of Clinical Execution experience, or Bachelor’s degree and 6 years of Clinical Execution experience, or Associate’s degree and 10 years of Clinical Execution experience, or high school diploma/GED and 12 years of Clinical Execution experience
7 years’ work experience in life sciences or medically related field, including 5 years of biopharmaceutical clinical research experience obtained leading global clinical trials in a biotech, pharmaceutical or CRO company
Experience managing direct reports across multiple geographies
Experience representing a sponsor company in regulatory audit/inspections
Experience at or oversight of outside clinical research vendors, including CROs, central labs, and imaging vendors
Sponsorship for this role is not guaranteed

Benefits

Comp & perks

A comprehensive employee benefits package, including a Retirement and Savings Plan with generous company contributions
Group medical, dental and vision coverage
Life and disability insurance
Flexible spending accounts
A discretionary annual bonus program
Stock-based long-term incentives
Award-winning time-off plans
Flexible work models where possible
Career development opportunities
Work/life balance support