Clinical Research Associate: Impactful Trials

AbbVie; Illinois; On-site; USD 70,000 - 100,000; Full time

Job summary

AbbVie is seeking a Clinical Research Associate (CRA) to join our team in Israel. The CRA will monitor activities at clinical sites to ensure that study protocols are followed and regulatory requirements are met.

You will collaborate with cross-functional teams to support site start-up, conduct, and close-out processes. The role requires on-site monitoring experience, strong knowledge of ICH/GCP, and the ability to train site personnel and manage investigator payments.

Qualifications

• 1–2+ years as a CRA in pharma or CRO.
• Experience conducting on-site monitoring of trials.
• Strong knowledge of ICH/GCP and local regulations.

Responsibilities

• Monitor clinical investigative sites to ensure adherence to study protocols.
• Ensure compliance with GCP, SOPs, and regulatory requirements.
• Conduct site qualification, initiation, interim monitoring and closeout visits.
• Oversee site personnel and coordinate action plans to maintain compliance.
• Ensure data quality and timely safety reporting from sites.
• Train site personnel on protocol requirements and regulatory obligations.
• Manage investigator payments and site agreements.

Skills

CRA experience

Site monitoring

Regulatory knowledge

GCP/ICH familiarity

Communication skills

Project management

Education

Health-related degree (Medicine/Life Sciences/Nursing)

Job description

AbbVie is seeking a Clinical Research Associate (CRA) to join our team in Israel. The CRA will monitor activities at clinical sites to ensure that study protocols are followed and regulatory requirements are met.

You will collaborate with cross-functional teams to support site start-up, conduct, and close-out processes. The role requires on-site monitoring experience, strong knowledge of ICH/GCP, and the ability to train site personnel and manage investigator payments.