Clinical Research Associate – Israel

About the role

AbbVie is looking for a Clinical Research Associate to support its clinical studies in Israel. The CRA will ensure successful execution of study protocols across all phases, from site start‑up to close‑out, while maintaining compliance with regulatory standards.

Key responsibilities

• Monitor clinical investigative sites to ensure adherence to study protocols and regulatory requirements.
• Conduct site qualification, initiation, interim monitoring, and close‑out visits for Phase 1–4 studies.
• Motivate and influence site personnel to meet study objectives without direct authority.
• Implement corrective action plans and maintain inspection readiness at assigned sites.
• Oversee data quality, timely safety reporting, and compliance with GCP, ICH guidelines, and AbbVie SOPs.
• Train site staff on protocol specifics and regulatory expectations.
• Manage investigator payments and negotiate agreements in line with contractual obligations.
• Identify and evaluate new investigators and clinical sites for future studies.

Required profile

• Experience monitoring Phase 1–4 clinical studies.
• Ability to manage multiple sites proactively and ensure compliance.
• Strong communication skills to train and influence site personnel.
• Capability to prepare and maintain expense reports and investigator payments.

Required skills

• Good Clinical Practice (GCP)
• ICH Guidelines
• AbbVie Standard Operating Procedures (SOPs)
• Regulatory compliance and inspection readiness
• Site monitoring and qualification processes