Join Everest Clinical Research as a Senior Clinical Research Associate, focusing on clinical trial monitoring in the West Region. Use your experience to ensure compliance and data integrity in ongoing studies.

In this key position, you will facilitate high-quality execution of clinical trials, engaging with study sponsors and medical sites across the USA. The role includes monitoring, site feasibility, and compliance oversight. Flexibility to travel 70% is necessary, prioritizing regions in the Pacific or Mountain zones.

Key Responsibilities:
• Conduct monitoring and track clinical trial status
• Coordinate site feasibility and attend Investigator Meetings
• Evaluate Investigator Site Files for document accuracy
• Submit comprehensive monitoring reports to management
• Assist with training and support for study staff

Requirements:
• Bachelor’s degree in a relevant life science
• Six years of clinical monitoring experience
• Proficient in ICH-GCP regulations
• Excellent verbal and written communication skills
• Ability to travel extensively as needed

Make a lasting impact on clinical research through your expertise at Everest.
#J-18808-Ljbffr

📌 Everest CRO Senior Clinical Research Associate (Manitoba)
🏢 Everest Clinical Research
📍 Manitoba