Advanced Clinical Research Associate - Site & Data Quality

AbbVie; Tandil; On-site; ARS 108,178,000 - 154,540,000; Full time

Job summary

AbbVie is seeking a Site Monitoring professional to advance our clinical trials by ensuring effective site engagement and high-quality data. You will collaborate with investigators and site staff, monitor trial conduct per protocol, and support recruitment strategies while maintaining patient safety and regulatory compliance.

The role emphasizes training junior CRAs, risk assessment, and using CRM tools to track progress across multiple sites, aligning with global standards and AbbVie SOPs.

Qualifications

• Bachelor's degree in health-related disciplines preferred.
• A minimum of 1 year clinically related experience, with 6 months in clinical research monitoring.
• Knowledge of regulatory requirements (ICH/GCP) and risk-based monitoring.
• Strong collaboration, planning and organizational skills.
• Ability to work effectively in a dynamic, multi-project environment.
• Excellent communication, presentation and problem-solving abilities.
• Mentorship capability to guide junior CRAs.

Responsibilities

• Act as primary contact for investigative sites and provide trial information.
• Align and motivate site staff and investigators on trial goals and patient treatment principles.
• Monitor sites per protocol with adherence to GCP, SOPs and regulatory standards.
• Utilize site engagement tools and CRM to report progress and measure impact.
• Link study protocols to site activities to support recruitment and retention.
• Ensure safety data reporting and site audit readiness.

Skills

Cross-functional collaboration

Project planning

Organizational skills

Site engagement

CRM tools

Risk-based monitoring

GCP/ICH knowledge

Communication skills

Presentation skills

Critical thinking

Education

Bachelor's Degree in health related disciplines

Tools

CRM software

Job description

AbbVie is seeking a Site Monitoring professional to advance our clinical trials by ensuring effective site engagement and high-quality data. You will collaborate with investigators and site staff, monitor trial conduct per protocol, and support recruitment strategies while maintaining patient safety and regulatory compliance.

The role emphasizes training junior CRAs, risk assessment, and using CRM tools to track progress across multiple sites, aligning with global standards and AbbVie SOPs.