Clinical Research Associate II: Site Partnerships

Allergan; Miami (FL); On-site; USD 85,000 - 120,000; Full time

Job summary

AbbVie in Miami is seeking a Clinical Research Monitoring professional to advance our trial programs by ensuring site performance, data integrity, and patient safety. You will partner with investigators and site staff to drive compliant, high-quality studies and to implement risk-based monitoring strategies.

This role requires a minimum year of experience in clinical research monitoring, deep knowledge of ICH/GCP, and strong cross-functional collaboration.

Qualifications

• Minimum 1 year of clinically related experience, with at least 6 months in clinical research monitoring.
• Knowledge of regulatory requirements (ICH/GCP) and risk-based monitoring.
• Ability to mentor junior CRAs and collaborate across functional teams.

Responsibilities

• Serve as primary contact for investigative sites and ensure protocol and patient safety compliance.
• Train and motivate site staff and investigators on trial goals and patient care principles.
• Monitor site performance, data integrity, and audit readiness in line with SOPs and regulations.
• Identify site risks and implement corrective actions with a customer-centric approach.

Job description

AbbVie in Miami is seeking a Clinical Research Monitoring professional to advance our trial programs by ensuring site performance, data integrity, and patient safety. You will partner with investigators and site staff to drive compliant, high-quality studies and to implement risk-based monitoring strategies.

This role requires a minimum year of experience in clinical research monitoring, deep knowledge of ICH/GCP, and strong cross-functional collaboration.