Global Site Management Lead, Clinical Trials

AbbVie; Irvine (CA); On-site; USD 140,000 - 190,000; Full time

Benefits offered by this job

Medical/dental/vision insurance

401(k) plan

Job summary

AbbVie in Irvine, CA seeks a Senior Site Management Lead to direct CSM integrity, quality and timely execution across assigned studies. You will influence with stakeholders, and manage site monitors within a global, matrix environment.

This role requires 5+ years of clinical research experience, strong leadership, and advanced MS Office skills. You will collaborate with study teams and country leaders to ensure successful study delivery and inspection readiness.

Qualifications

• Bachelor’s degree in a (para)medical or scientific field; incumbent has 5+ years of industry clinical research experience.
• Experience leading global studies and directing site management activities in a matrix environment.
• Excellent written and verbal communication skills with ability to influence stakeholders.

Responsibilities

• Drive study level global and area level CSM deliverables with timelines and resources.
• Analyze study timelines and confirm CSM feasibility; communicate resource needs to Country Leaders.
• Lead site monitoring strategy, Site Engagement Strategy, and TMF completeness for CSM artifacts.
• Oversee monitoring activities and ensure quality deliverables and milestone adherence.
• Collaborate with other SMLs and stakeholders to manage risks and escalate issues.
• Ensure on-going CSM Inspection Readiness from study start to close.

Skills

Clinical research

Leadership

Communication

Influence without authority

MS Office suite

Education

Bachelor’s Degree in (para)medical or scientific field

Tools

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Microsoft OneNote

Job description

AbbVie in Irvine, CA seeks a Senior Site Management Lead to direct CSM integrity, quality and timely execution across assigned studies. You will influence with stakeholders, and manage site monitors within a global, matrix environment.

This role requires 5+ years of clinical research experience, strong leadership, and advanced MS Office skills. You will collaborate with study teams and country leaders to ensure successful study delivery and inspection readiness.