Senior Clinical Research Associate: Site Lead

BioSpace; Sofia (NM); Presencial; USD 100.000 - 140.000; Jornada completa

Descripción de la vacante

AbbVie is seeking an experienced clinical research professional to advance our trials by partnering with investigative sites and study teams. You will drive site engagement, ensure protocol compliance, and leverage CRM tools to optimize data quality and patient safety.

Responsibilities include mentoring CRAs, monitoring site performance, and collaborating across functions to deliver high-quality study outcomes while maintaining regulatory and ethical standards.

Formación

• Experience in site engagement and site management for clinical trials.
• Knowledge of GCP, ICH guidelines and regulatory requirements.
• Ability to train and mentor CRAs and site staff.

Responsabilidades

• Serve as the primary point of contact for investigative sites, ensuring clear communication.
• Align site staff and investigators with trial goals, protocol, and patient care principles.
• Monitor site activities for protocol compliance, safety, and data integrity.
• Gather local insights and report progress using CRM tools to measure impact.
• Connect study protocols with scientific principles to enable compliant execution.
• Support patient recruitment and retention through strategy and training.
• Mentor junior CRAs and participate in local/global task forces as needed.
• Assess risks proactively with Central Monitoring to prevent issues.
• Develop risk mitigation plans and drive corrective actions when necessary.
• Identify new investigators/sites to support trial placement.

Conocimientos

Site engagement

Cross-functional

Risk-based monitoring

GCP knowledge

Stakeholder communication

Educación

Bachelor's or higher in health sciences

Clinical research certification

Descripción del empleo

AbbVie is seeking an experienced clinical research professional to advance our trials by partnering with investigative sites and study teams. You will drive site engagement, ensure protocol compliance, and leverage CRM tools to optimize data quality and patient safety.

Responsibilities include mentoring CRAs, monitoring site performance, and collaborating across functions to deliver high-quality study outcomes while maintaining regulatory and ethical standards.