Senior Clinical Research Associate: Site Partnerships

AbbVie; California; Presencial; USD 110.000 - 150.000; Jornada completa

Descripción de la vacante

AbbVie seeks a Clinical Research Monitor to partner with investigative sites, training staff on trial objectives and ensuring protocol compliance across study activities. You will coordinate risk assessments and drive site performance while maintaining patient safety and data integrity.

The role emphasizes collaboration with investigators, monitoring teams, and stakeholders to optimize trial execution and quality across sites in the United States, with a focus on adherence to GCP and regulatory

Formación

• Appropriate tertiary qualification in health related disciplines (Medical, Scientific, Nursing) preferred.
• Minimum of 1 year of clinically related experience in clinical research monitoring.
• Familiar with risk-based monitoring approaches, on-site and off-site monitoring.

Responsabilidades

• Primary point of contact for the investigative site in clinical trials.
• Explain protocol goals and patient treatment principles to site staff and PI.
• Monitor compliance with protocol, SOPs, and ICH/GCP guidelines.
• Report risk signals and collaborate with Central Monitoring to address site risks.

Conocimientos

Site engagement

Risk-based monitoring

Cross-functional collaboration

GCP/ICH knowledge

Data integrity

Educación

Health-related degree (Medical, Scientific, Nursing)

Descripción del empleo

AbbVie seeks a Clinical Research Monitor to partner with investigative sites, training staff on trial objectives and ensuring protocol compliance across study activities. You will coordinate risk assessments and drive site performance while maintaining patient safety and data integrity.

The role emphasizes collaboration with investigators, monitoring teams, and stakeholders to optimize trial execution and quality across sites in the United States, with a focus on adherence to GCP and regulatory