CRA II: Site Partnerships & Monitoring

AbbVie; United States; On-site; USD 90,000 - 120,000; Full time

Job summary

AbbVie seeks a Clinical Research Associate to partner with investigative sites across the United States. This role monitors trials, trains site staff, evaluates protocol adherence and ensures data integrity and safety; collaboration with cross‑functional teams is essential.

You will mentor junior CRAs, manage site relationships, and report findings with focus on patient safety, timeline milestones and quality outcomes in a fast-paced environment.

Qualifications

• Minimum 1 year of clinically related experience; risk-based monitoring familiarity.
• Knowledge of therapeutic area indications and clinical trial requirements.
• Experience collaborating with internal and external stakeholders to drive study execution.

Responsibilities

• Primary point of contact for investigative sites; provide contextual information on trials.
• Aligns and trains site staff and investigators on trial goals, protocol, and patient treatment principles.
• Conducts site evaluation, training, monitoring, and site closure activities per protocol and GCPs.
• Gather local/site insights and use CRM tools to report progress and measure impact of engagement strategies.
• Mentor and train less experienced CRAs; participate in local/global task forces as assigned.
• Monitor risk signals with Central Monitoring; implement preventive and corrective actions to ensure safety and data integrity.
• Identify and evaluate potential investigators/sites for future studies; manage investigator payments as applicable.

Skills

Site monitoring

Regulatory knowledge

Therapeutic knowledge

Cross-functional collaboration

Project planning

Communication skills

Education

Healthcare degree

GCP familiarity

Tools

CRM tool

Job description

AbbVie seeks a Clinical Research Associate to partner with investigative sites across the United States. This role monitors trials, trains site staff, evaluates protocol adherence and ensures data integrity and safety; collaboration with cross‑functional teams is essential.

You will mentor junior CRAs, manage site relationships, and report findings with focus on patient safety, timeline milestones and quality outcomes in a fast-paced environment.