Global Site Management Lead

Allergan; Irvine (CA); On-site; USD 180,000 - 240,000; Full time

Benefits offered by this job

401(k) plan

Job summary

AbbVie in Irvine, CA is seeking a Senior Clinical Site Management Lead to provide direction and operational excellence for CSM activities across global studies. This role may serve as the overall study strategy leader or manage area site execution in collaboration with other SMLs.

You will drive site monitoring, risk management, TMF completeness, and liaison between site monitors and the study team. Strong communication, leadership, and ICH/global regulations expertise are required.

Qualifications

• Bachelor’s degree or equivalent in a (para)medical or scientific field.
• Strong communication and leadership abilities; able to influence in a matrix environment.
• English fluency with excellent planning and organizational skills.

Responsibilities

• Drive study-level and area-level CSM deliverables with timelines and resources.
• Lead site monitoring strategy, engagement, and TMF completeness.
• Collaborate with Clinical Study Team, Country Leaders, and other SMLs to mitigate risk and ensure compliance.
• Ensure study timelines across the lifecycle and effective site execution responsibilities.
• Provide inputs on CSM documents and drive TMF completeness for CSM artifacts.

Skills

Communication skills

Leadership

Influence without authority

Presentation skills

English fluency

Planning and organization

Education

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

Tools

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Microsoft OneNote

Job description

AbbVie in Irvine, CA is seeking a Senior Clinical Site Management Lead to provide direction and operational excellence for CSM activities across global studies. This role may serve as the overall study strategy leader or manage area site execution in collaboration with other SMLs.

You will drive site monitoring, risk management, TMF completeness, and liaison between site monitors and the study team. Strong communication, leadership, and ICH/global regulations expertise are required.