Study Delivery Sr Mgr (Study Delivery Lead)

Amgen

23h

About The Position

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. With our focus on four therapeutic areas –Oncology, Inflammation, General Medicine, and Rare Disease– we reach millions of patients each year. 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. Study Delivery Senior Manager - Study Delivery Lead What you will do Let’s do this. Let’s change the world. In this vital role, you will take ownership of global clinical trial delivery, translating product and clinical objectives into executable plans that enable delivery of timely, high-quality data, in support of Amgen’s mission to serve patients. Own end-to-end delivery of assigned 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 inclusive of feasibility, site selection, site engagement, recruitment and retention, and vendor delivery. Proactively identify and manage study risks, driving 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 where needed. Provide clear leadership, direction, and escalation management to resolve complex study issues across geographies. Build strong partnerships with internal stakeholders and external vendors, ensuring effective collaboration and performance. Champion continuous improvement, innovation, and regulatory compliance across all phases of clinical trial delivery. What we expect of you We are all different, yet we all use our unique contributions to serve patients. The candidate we seek is an individual with the following qualifications.

Requirements

• Doctorate degree and 2 years of Clinical Execution experience
• Master’s degree and 4 years of Clinical Execution experience
• Bachelor’s degree and 6 years of Clinical Execution experience
• Associate’s degree and 10 years of Clinical Execution experience
• High school diploma / GED and 12 years of Clinical Execution experience

Nice To Haves

• 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 (CRO’s, central labs, imaging vendors, etc.)

Responsibilities

• Own end-to-end delivery of assigned 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 inclusive of feasibility, site selection, site engagement, recruitment and retention, and vendor delivery.
• Proactively identify and manage study risks, driving 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 where needed.
• Provide clear leadership, direction, and escalation management to resolve complex study issues across geographies.
• Build strong partnerships with internal stakeholders and external vendors, ensuring effective collaboration and performance.
• Champion continuous improvement, innovation, and regulatory compliance across all phases of clinical trial delivery.

Benefits

• 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, and flexible spending accounts
• A discretionary annual bonus program, or for field sales representatives, a sales-based incentive plan
• Stock-based long-term incentives
• Award-winning time-off plans
• Flexible work models where possible.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree