Study Delivery Sr Mgr (Study Delivery Lead)

Overview

Take ownership of global clinical trial delivery, translating product and clinical objectives into executable plans that deliver timely, high-quality data, and lead cross-functional study teams to execute them.

What you'll do

• 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 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.

Nice to have

• 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.).

Details

• Location: United States - Remote.
• Expected annual salary range in the U.S. (excluding Puerto Rico): $163,721 USD to $197,116 USD, varying by relevant skills, experience, and qualifications.
• Sponsorship for this role is not guaranteed.