Oncology CRA II — Trusted Site Partner

AbbVie; Maryland; On-site; USD 70,000 - 110,000; Full time

Benefits offered by this job

Paid time off

Medical/dental/vision insurance

401(k)

Job summary

AbbVie in Maryland is seeking an experienced Clinical Research Associate to advance AbbVie's clinical research program by ensuring protocol compliance, data integrity, and patient safety across sites. This role emphasizes site engagement, monitoring visits, training site staff, and proactive risk assessment in a collaborative, cross-functional environment.

The ideal candidate will have a life sciences degree, 1+ year of clinical monitoring experience, and strong knowledge of ICH/GCP guidelines.

Qualifications

• Bachelor's degree in a life sciences field or related discipline.
• Minimum 1 year of clinically related experience, with monitoring of trials preferred.
• Knowledge of ICH/GCP guidelines and regulatory requirements.
• Strong cross-functional collaboration and communication skills.
• Experience training and mentoring junior CRAs is a plus.

Responsibilities

• Primary point of contact for investigative sites and stakeholders.
• Train and motivate site staff on trial goals and patient treatment principles.
• Conduct site evaluations, training, monitoring activities with regulatory compliance.
• Engage sites using CRM tools to report progress and measure impact.
• Support patient recruitment, protocol adherence and data integrity.
• Identify and escalate site risks and implement corrective actions.

Skills

Site engagement

CRA experience

Regulatory knowledge

Cross-functional collaboration

Communication skills

Education

Bachelor's degree in life sciences

Tools

CRM software

Job description

AbbVie in Maryland is seeking an experienced Clinical Research Associate to advance AbbVie's clinical research program by ensuring protocol compliance, data integrity, and patient safety across sites. This role emphasizes site engagement, monitoring visits, training site staff, and proactive risk assessment in a collaborative, cross-functional environment.

The ideal candidate will have a life sciences degree, 1+ year of clinical monitoring experience, and strong knowledge of ICH/GCP guidelines.