Global Clinical Site Management Lead

Abbvie; Maidenhead; On-site; GBP 70,000 - 100,000; Full time

Job summary

AbbVie UK is seeking an experienced SML, reporting to the Associate Director/Sr. Manager, Global Site Management, to guide CSM integrity, quality and timeliness of activities across assigned studies.

The role may lead the overall CSM strategy or manage area site execution in collaboration with other SMLs. You will drive study-level strategies, monitor timelines, engage sites, coordinate risk assessments, and ensure TMF completeness.

Qualifications

• Bachelor’s Degree or equivalent in a (para)medical or scientific field.
• Minimum of 5 years of industry clinical research experience.
• Experience in monitoring or project management on global studies.
• Fluent written and spoken English; strong communication skills.
• Ability to influence in a matrix environment and lead initiatives.
• Familiarity with SOPs, ICH, and global regulations.

Responsibilities

• Analyze study timelines and confirm deliverables for CSM feasibility.
• Support CSM resource planning with country leaders.
• Lead study-level site monitoring strategy and activation.
• Set and drive Site Engagement Strategy and TMF completeness.
• Oversee site monitoring activities and risk management plans.
• Ensure timely study milestones and close-out activities.
• Collaborate across study teams to address risks and issues.

Skills

Communication skills

Leadership

Influence without authority

Project management

English fluency

Analytical thinking

Cross-functional collaboration

Education

Bachelor's degree in medical/science field

Tools

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Microsoft OneNote

Job description

AbbVie UK is seeking an experienced SML, reporting to the Associate Director/Sr. Manager, Global Site Management, to guide CSM integrity, quality and timeliness of activities across assigned studies.

The role may lead the overall CSM strategy or manage area site execution in collaboration with other SMLs. You will drive study-level strategies, monitor timelines, engage sites, coordinate risk assessments, and ensure TMF completeness.