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
- Strong organizational capabilities
- Mastery of Microsoft Office tools
- Valid driver's license and passport needed Capitalize on your clinical expertise to support AbbVie in delivering innovative medical solutions to patients.
📌 Clinical Research Associate II Position (Edmonton)
🏢 Allergan
📍 Edmonton
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