Drive clinical excellence as a Clinical Research Associate II at AbbVie. This role emphasizes the oversight of clinical site operations to ensure studies meet strict protocol standards. Dedicated to transforming lives, AbbVie is seeking a skilled with two years of monitoring experience to enhance our R&D; capabilities. You will be responsible for conducting training, managing site compliance, and safeguarding the quality of data collected throughout clinical trials. Key Responsibilities:
Monitor clinical study execution for protocol adherence
Facilitate site initiation and closeout processes
Engage site personnel to meet research goals
Ensure updated safety reporting and compliance
Train sites on regulatory requirements and protocols Requirements:
Minimum of 2 years clinical monitoring experience
Proficient in ICH guidelines and GCPs
Robust organizational capabilities
Mastery of Microsoft Office tools
Valid driver's license and passport needed Capitalize on your clinical expertise to support AbbVie in delivering creative medical solutions to patients.

📌 Clinical Research Associate Ii Position Edmonton
🏢 Allergan
📍 Edmonton