Elevate your career with Everest Clinical Research as a Senior Clinical Research Associate in the West Region. Bring your clinical trial expertise and monitoring skills to a agile, customer-focused team. This role requires substantial experience in clinical monitoring, with a focus on regulatory compliance and study progress tracking.

You will interact with investigators, manage site files, and ensure integrity in clinical data throughout trials. Successful candidates must be ready to travel up to 70% within the USA, ideally in the Pacific or Mountain time zones. Key Responsibilities:

- Monitor and report on clinical trial progress
- Perform feasibility assessments and site initiation visits
- Train site staff and assist with study inquiries
- Review Investigator Site Files for compliance
- Prepare monitoring visit reports and expense submissions Requirements:
- Bachelor’s degree in life sciences or related field
- Minimum of six years monitoring experience
- In-depth knowledge of ICH-GCP guidelines
- Strong communication and organizational skills
- Valid driver’s license and travel readiness Utilize your expertise in clinical trials, compliance, and monitoring to drive success at Everest.

📌 Senior Clinical Research Associate Remote (Canada)
🏢 Everest Clinical Research
📍 Canada