Central Monitor - Remote

Overview

The Central Monitor plays a pivotal role in AbbVie’s risk-based quality management initiative, focusing on early identification of risks in clinical studies through macro-level data analysis.

In Short

• Analyze near-real-time aggregate clinical and operational data.
• Utilize Key Risk Indicators and Quality Tolerance Limits to identify risks.
• Document detected issues and translate them into simple language.
• Communicate findings to cross-functional stakeholders.
• Support primary site monitors with critical information.
• Collaborate with study teams to ensure quality.
• Participate in risk management meetings.
• Contribute to the development of RBM systems.
• Champion RBQM processes across AbbVie.
• Work on multiple-jurisdiction studies globally.

Requirements

• Bachelor’s degree in a related field.
• Minimum 3 years in clinical research monitoring.
• Experience in an RBQM model is preferred.
• Knowledge of therapeutic indications and ICH/GCP guidelines.
• Strong analytical and root cause analysis skills.
• Ability to develop contingency plans.
• Adaptability to new problems.
• Excellent planning and organizational skills.
• Ability to work independently.

Benefits

• Equal opportunity employer.
• Commitment to integrity and innovation.
• Diverse and inclusive work environment.