Bilingual Clinical Research Associate II - Remote

Overview

As a Bilingual Clinical Research Associate II at AbbVie, you will monitor clinical investigative sites and ensure compliance with regulations and quality standards, contributing to the successful execution of clinical studies.

In Short

• Monitor clinical study activities at investigative sites.
• Conduct site qualification, initiation, monitoring, and closeout visits.
• Ensure compliance with regulations and Good Clinical Practices (GCP).
• Oversee site personnel and manage action plans for compliance.
• Ensure quality and timely submission of study data.
• Train site personnel on protocols and regulatory requirements.
• Manage investigator payments and negotiate agreements.
• Identify and evaluate potential new investigators/sites.

Requirements

• Health-related tertiary qualification preferred.
• Minimum 2 years of clinical monitoring experience.
• Knowledge of ICH/GCP Guidelines and clinical trial regulations.
• Strong organizational and planning skills.
• Analytical and interpersonal skills with clear communication abilities.
• Ability to travel at least 50% of the time.

Benefits

• Work with a dedicated team impacting patient lives.
• Opportunity to be part of a recognized workplace.
• Engagement in groundbreaking science and research.