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Job Description & How to Apply Below
This role requires a Bachelor's degree and a minimum of 4-6 years of CRA experience within pharmaceutical or CRO settings. You’ll conduct site monitoring, support study phases, and resolve site issues to align with study objectives. Strong organizational and communication skills are essential for managing relationships successfully.
Key Responsibilities:
• Conduct monitoring activities for clinical sites
• Support site initiation and study closeout visits
• Ensure compliance with protocols and regulations
• Build strong relationships with investigative sites
• Identify and resolve issues while meeting timelines
Requirements:
• Bachelor’s degree required
• 4-6 years of CRA experience in relevant environments
• Experience monitoring clinical trials PI-IV
• Strong knowledge of GCP guidelines
• Willingness to travel up to 75% in Western Canada
Utilize your clinical research expertise at Solomon Page to contribute to impactful studies in Western Canada.
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Position Requirements
10+ Years
work experience
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