Oncology Clinical Research Associate II - Elevate Trials

Oncology Voice Network LLC; Milford, Northern (CT, KY); Hybrid; USD 90,000 - 120,000; Full time

Benefits offered by this job

Dental insurance

Paid time off

Health insurance

Job summary

AbbVie seeks a dedicated Clinical Research Associate to support site engagement and monitoring across therapeutic areas. You will ensure high quality data, patient safety, and protocol adherence while training site staff and coordinating with investigators.

The role requires advanced knowledge of GCP/ICH, risk-based monitoring, and strong cross-functional collaboration. A health-related degree and clinical monitoring experience are preferred.

Qualifications

• Appropriate tertiary qualification in health related disciplines preferred.
• Experience in clinical research monitoring and site engagement.
• Knowledge of ICH/GCP guidelines and regulatory expectations.

Responsibilities

• Serve as primary point of contact for investigative sites and ensure data integrity and patient safety.
• Align site staff and investigators with trial goals, protocol, and patient treatment principles.
• Conduct site evaluations, training, monitoring activities in line with SOPs and regulations.
• Utilize CRM tools to report progress and measure impact of site engagement strategies.
• Mentor junior CRAs and participate in global/local task forces as needed.
• Identify/site risk signals and implement preventative or corrective actions.

Skills

Clinical monitoring

Risk-based monitoring

Regulatory knowledge

Cross-functional collaboration

Communication skills

Project planning

Presentation skills

Education

Health-related degree

Tools

CRM systems

Regulatory databases

Job description

AbbVie seeks a dedicated Clinical Research Associate to support site engagement and monitoring across therapeutic areas. You will ensure high quality data, patient safety, and protocol adherence while training site staff and coordinating with investigators.

The role requires advanced knowledge of GCP/ICH, risk-based monitoring, and strong cross-functional collaboration. A health-related degree and clinical monitoring experience are preferred.