Clinical Research Associate II

Job Description

To enable AbbVie’s emergence as a world class R&D organization, the Clinical Site Manager anticipates and proactively solves study-related clinical site issues as they occur and initiates, recommends, and communicates corrective action ensuring successful protocol level execution of Clinical Site Management deliverables involving start‑up, execution, and close‑out of studies.

Responsibilities

• Monitors site activities related to AbbVie clinical studies to ensure successful execution of the protocol and adherence to federal, local regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie SOPs, Monitoring Plans, and quality standards.
• Conducts site qualification, initiation, interim monitoring, and study close‑out visits for Phase I to III studies in accordance with regulations, GCPs, ICH Guidelines, and AbbVie SOPs.
• Oversees site personnel activities, motivates and influences them to meet study objectiv...