Elevate your career with ICON Strategic Solutions as a Clinical Research Associate. Embrace a supportive, sponsor-dedicated environment focused on phases II-IV of clinical studies.
At ICON, a leader in FSP services, you will contribute to vital clinical research alongside experienced CRAs. You'll independently set up, monitor, and close investigational sites, ensuring compliance with ICH-GCP regulations. Your proactive approach will enhance study cost efficiency and support the training of junior CRAs, promoting a team-oriented culture.
Key Responsibilities:
• Set up and monitor clinical studies independently
• Submit protocol and consent documents for approval
• Take responsibility for study cost efficiency
• Review study documentation and conduct feasibility studies
• Assist in training and mentoring junior CRAs
Requirements:
• 18 months+ monitoring experience in phases I-III
• Previous medium-sized study monitoring experience
• Knowledge of ICH-GCP guidelines
• Ability to meet tight deadlines
• Availability for 60% travel with a valid driving license
Maximize your impact in clinical research with ICON’s global expertise.
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📌 Clinical Research Associate at ICON Solutions (Toronto)
🏢 ICON Strategic Solutions
📍 Toronto