Clinical Research Associate: Site Liaison & Data Integrity

AbbVie Inc.; Los Angeles (CA); Presencial; USD 90.000 - 120.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Paid time off

Medical/dental/vision insurance

401(k)

Descripción de la vacante

AbbVie Inc. in the United States seeks a site-focused clinical research professional to coordinate trial activities, ensure protocol adherence, and maintain data integrity across sites.

You will train site staff, monitor performance, manage investigator payments, and ensure regulatory compliance while safeguarding patient safety and driving quality study execution through collaborative engagement with investigators and CRM tools.

Formación

• Appropriate tertiary qualification in health related disciplines or equivalent experience.
• Clinical research coordinating experience preferred.
• Knowledge of regulatory requirements (ICH/GCP) is preferred.
• Ability to work cross-functionally and manage multiple projects.

Responsabilidades

• Act as primary contact for investigative sites and align staff with trial goals.
• Monitor site performance, conduct training, and ensure protocol compliance.
• Ensure data integrity, safety reporting and timely data submission.
• Manage investigator payments and regulatory documentation.

Conocimientos

Clinical research

Cross-functional collaboration

Planning & organization

Communication skills

Integrity & ethics

Educación

Bachelor’s degree in health/related field

Herramientas

CRM tool

Descripción del empleo

AbbVie Inc. in the United States seeks a site-focused clinical research professional to coordinate trial activities, ensure protocol adherence, and maintain data integrity across sites.

You will train site staff, monitor performance, manage investigator payments, and ensure regulatory compliance while safeguarding patient safety and driving quality study execution through collaborative engagement with investigators and CRM tools.