Oncology Clinical Research Associate II – Site Excellence

AbbVie; Wisconsin; Remote; USD 90,000 - 130,000; Full time

Job summary

AbbVie is seeking a Clinical Research Associate (CRA) experienced in site engagement and monitoring to advance our clinical trials. You will partner with investigators and site staff to ensure protocol adherence, data quality, and patient safety.

You will train and mentor CRAs, optimize site strategies, and drive recruitment while maintaining compliance with ICH/GCP and AbbVie SOPs. This role requires collaboration across functions in a fast-paced environment.

Qualifications

• Bachelor’s degree in health-related disciplines preferred.
• Minimum 1 year of clinically related experience, including 6 months in clinical research monitoring.
• Familiar with risk-based monitoring, onsite and offsite monitoring.
• Strong cross-functional collaboration skills among internal and external stakeholders.
• Strong planning and organizational skills in a dynamic environment.
• Advanced regulatory and ICH/GCP knowledge and applicable policies.
• Ability to leverage technology and resources to provide customer-centric site support.
• Excellent interpersonal skills with written, verbal, and presentation abilities.
• Apply good judgment to address clinical site issues with integrity.
• Self-motivated, delivering timely and quality outcomes in a fast-paced environment.

Responsibilities

• Primary point of contact for investigative sites and provide context on trials.
• Align, train and motivate site staff and principal investigators.
• Conduct site evaluation, training, monitoring per protocol and regulatory plans.
• Develop site engagement strategies and report progress using CRM tools.
• Connect protocol and clinical science to day-to-day trial execution and recruitment plans.
• Mentor CRAs and participate in global/local initiatives as assigned.
• Proactively monitor risks in collaboration with Central Monitoring.
• Think critically to resolve site risk signals and implement corrective actions.
• Identify new investigators/sites to support study placement.
• Ensure data quality and timely reporting, manage site payments as applicable.

Skills

Cross-functional collaboration

Planning & organization

Regulatory compliance knowledge

Site engagement strategy

Data integrity focus

Mentoring CRAs

Critical thinking

Risk assessment

CRM tools

Communication skills (written/verbal)

Education

Bachelor’s degree in health/science

Tools

CRM tool

Job description

AbbVie is seeking a Clinical Research Associate (CRA) experienced in site engagement and monitoring to advance our clinical trials. You will partner with investigators and site staff to ensure protocol adherence, data quality, and patient safety.

You will train and mentor CRAs, optimize site strategies, and drive recruitment while maintaining compliance with ICH/GCP and AbbVie SOPs. This role requires collaboration across functions in a fast-paced environment.