Global Site Management Lead - Clinical Trials Strategy

AbbVie; Illinois; On-site; USD 120,000 - 180,000; Full time

Benefits offered by this job

401(k)

Paid time off

Medical/dental/vision insurance

Long-term incentives

Job summary

In this role you will manage site monitors in a matrix environment, drive risk assessment and mitigation, and contribute to TMF completeness and inspection readiness from study start to close. A Bachelor’s degree and 5+ years of clinical research experience are required.

Qualifications

• Bachelor's Degree or equivalent in a (para)medical or scientific field.
• 5+ years of industry clinical research experience including 2 years of monitoring or project management on a global study.
• Preferred exposure in study initiation through study completion in multiple phases.
• Demonstrates a high level of core and technical competencies through management of clinical trials.
• Good written and verbal communication skills including fluency in English; strong presentation skills.

Responsibilities

• Accountable for driving study level global and/or area level CSM deliverables by targeted timelines with allocated resources for their assigned studies.
• Analyze study timelines and assumptions to confirm feasibility for CSM; support CSM resource needs with Country Leaders.
• Lead study-level site monitoring strategy and Site Engagement Strategy.
• Oversee monitoring activities to ensure quality deliverables, track status, and milestone adherence; drive CSM activities at site level.
• Ensure site compliance, elevate issues, analyze trends for continuous improvement.
• Provide inputs on CSM documents at the study level and drive TMF completeness for CSM artifacts.
• Ensure ongoing CSM Inspection Readiness activities throughout the study.

Skills

Communication skills

Leadership

English fluency

Project management

Microsoft Office

Education

Bachelor's Degree

Tools

Microsoft Word

Microsoft PowerPoint

Microsoft Excel

Microsoft OneNote

Job description

In this role you will manage site monitors in a matrix environment, drive risk assessment and mitigation, and contribute to TMF completeness and inspection readiness from study start to close. A Bachelor’s degree and 5+ years of clinical research experience are required.