Elevate your career with ICON Strategic Solutions as a Clinical Research Associate. Embrace a supportive, sponsor-dedicated setting 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 cooperative 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. #J-18808-Ljbffr

📌 Clinical Research Associate At Icon Solutions Winnipeg (Canada)
🏢 ICON Strategic Solutions
📍 Canada