Senior Clinical Research Associate

📋 Description

• Primary Sponsor point of contact for investigative sites.
• Mentor and align monitoring staff with trial goals.
• Conduct site evaluation, training, and monitoring per GCP/ICH.
• Tailor site engagement strategy; track progress and impact.
• Support recruitment/retention based on disease journey.
• Ensure data quality and regulatory inspection readiness.

🎯 Requirements

• Relevant tertiary health qualification preferred.
• 3+ years in clinical research monitoring; risk-based monitoring.
• Knowledge of therapeutic areas and regulatory/ICH/GCP rules.
• Strong communication and cross-functional collaboration.
• Excellent planning, organization, and multitasking.
• Ability to leverage tech/tools to support site operations.

🎁 Benefits

• AbbVie is an equal opportunity employer.