Clinical Research Associate I: Kickstart Your Trials Career

AbbVie Inc.; Sydney; On-site; AUD 90,000 - 120,000; Full time

Job summary

AbbVie Australia is seeking a Clinical Research Associate I to join our expanding clinical operations team in Australia. You will monitor investigational sites for Phase 1–4 studies, ensure GCP/ICH compliance, and support data quality and safety reporting.

This role focuses on on-site monitoring, site qualification/initiation/closeout visits, and investigator payments in a collaborative environment. We value flexibility, professional growth, and a commitment to ethical, high-quality clinical

Qualifications

• 1 year clinically related experience with 6 months in clinical research monitoring.
• On-site monitoring of investigational drug or device trials required.
• Knowledge of clinical trial regulations (ICH/GCP) and applicable rules.
• Strong planning and organizational skills in a dynamic environment.
• Ability to work with cross-functional teams and follow processes.
• Excellent communication and problem-solving abilities.
• Demonstrated business ethics and integrity.

Responsibilities

• Monitor sites to ensure protocol adherence and regulatory compliance.
• Conduct site qualification, initiation, interim monitoring and closeout visits.
• Ensure data quality and timely reporting of safety events.
• Train site personnel on protocol and regulatory requirements.
• Manage investigator payments and own expense reports.
• Identify and evaluate potential investigators/sites continuously.
• Report adverse events within 24 hours and ensure safety reporting.
• Maintain regulatory inspection readiness and adherence to codes.

Skills

Clinical monitoring

GCP/ICH knowledge

Planning & organization

Analytical thinking

Communication skills

Ethics & integrity

Team collaboration

Education

Health-related degree

Job description

AbbVie Australia is seeking a Clinical Research Associate I to join our expanding clinical operations team in Australia. You will monitor investigational sites for Phase 1–4 studies, ensure GCP/ICH compliance, and support data quality and safety reporting.

This role focuses on on-site monitoring, site qualification/initiation/closeout visits, and investigator payments in a collaborative environment. We value flexibility, professional growth, and a commitment to ethical, high-quality clinical