Global Site Management Lead - Clinical Trials

AbbVie; Maidenhead; On-site; GBP 70,000 - 110,000; Full time

Job summary

AbbVie in Maidenhead seeks an experienced Senior Manager to lead Clinical Site Management strategy and ensure timely, high-quality CSM deliverables across studies. The role can drive study-level site monitoring and collaborate with global SMLs and country teams to align timelines and resources.

You will develop and own the Site Monitoring Plan, Site Engagement Strategy, and TMF artifacts, guiding study execution from initiation to close out while managing risks with RAMP.

Qualifications

• Bachelor’s Degree or equivalent OUS degree in (para)medical or scientific field
• 5+ years of industry clinical research experience and preferred 2 years of monitoring or project management on a global study
• Fluency in English with excellent written and verbal communication skills
• Competent in SOPs, ICH, Global Regulations, Ethics and Compliance

Responsibilities

• Analyze study timelines and overall study assumptions to confirm deliverables are feasible for CSM
• Support and communicate CSM resource needs with Country Leaders in alignment with study deliverables and milestones
• Accountable for study level site monitoring strategy, documented in Site Monitoring Plan
• Lead Site Engagement Strategy and ensure timely milestones across study lifecycle
• Drive site-level activities including site selection, activation, engagement, protocol adherence and close out
• Oversee monitoring activities at study/area level with other SMLs to ensure quality and milestone adherence
• Identify and mitigate risks with RAMP and collaborate with Clinical Study Team to address issues
• Ensure TMF completeness for CSM artifacts and inspection readiness

Skills

Presentation skills

English proficiency

Communication skills

Education

Bachelor’s Degree or equivalent

Tools

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Microsoft OneNote

Job description

AbbVie in Maidenhead seeks an experienced Senior Manager to lead Clinical Site Management strategy and ensure timely, high-quality CSM deliverables across studies. The role can drive study-level site monitoring and collaborate with global SMLs and country teams to align timelines and resources.

You will develop and own the Site Monitoring Plan, Site Engagement Strategy, and TMF artifacts, guiding study execution from initiation to close out while managing risks with RAMP.