Bilingual Clinical Research Associate II - Remote

Overview

As a Bilingual Clinical Research Associate II at AbbVie, you will play a crucial role in ensuring the successful execution of clinical studies while adhering to regulatory standards and promoting the well-being of study participants.

In Short

• Monitor clinical investigative sites for adherence to protocols.
• Conduct site qualification, initiation, and closeout visits.
• Manage site personnel and ensure compliance with regulations.
• Ensure quality and timely submission of study data.
• Train site personnel on protocols and regulatory requirements.
• Negotiate investigator agreements and manage payments.
• Identify and evaluate potential new study sites.
• Travel at least 50% of the time for site visits.

Requirements

• Tertiary qualification in a health-related field preferred.
• Minimum 2 years of monitoring experience in clinical trials.
• Knowledge of therapeutic indications related to clinical trials.
• Understanding of clinical research regulations and GCP.
• Strong organizational and planning skills.
• Excellent communication and interpersonal skills.
• Demonstrated business ethics and integrity.
• Proficiency in Microsoft Office Suite.

Benefits

• Work in a leading global biopharmaceutical company.
• Opportunity to impact patient lives positively.
• Collaborative work environment with talented professionals.
• Career development opportunities in a dynamic setting.