Elevate your clinical research career as a Clinical Research Associate! Manage and monitor studies in phases II and III while ensuring compliance and integrity throughout the study lifecycle.

In this pivotal role, you'll focus on overseeing clinical studies, maintaining adherence to GCP, and building robust relationships with investigators. Your responsibilities will include the qualification and initiation of study sites, alongside supervising the study conduct to ensure regulatory compliance. Your role is vital to the success of clinical research initiatives.

Key Responsibilities
Oversee monitoring of clinical studies in phases II-III
Ensure compliance with Positive Clinical Practices
Identify and initiate investigators and their sites
Supervise study conduct in line with regulations
Manage adherence to study procedures and integrity

Requirements:
Bachelor's degree in life sciences
Minimum 1 year of CRA experience in relevant settings
Experienced in site initiation and close-out processes
Clinical study experience in phases II-III
Excellent English communication proficiency

Bring your expertise in monitoring and compliance to advance clinical research and support creative treatments.

📌 Clinical Research Associate For Regulatory Compliant Trials Ottawa (Canada)
🏢 Resourcing Life Science
📍 Canada