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 statusCoordinate site feasibility and attend Investigator MeetingsEvaluate Investigator Site Files for document accuracySubmit comprehensive monitoring reports to managementAssist with training and support for study staffRequirements:Bachelor's degree in a relevant life scienceSix years of clinical monitoring experienceProficient in ICH-GCP regulationsExcellent verbal and written communication skillsAbility to travel extensively as neededMake a lasting impact on clinical research through your expertise at Everest.

📌 Everest Cro Senior Clinical Research Associate (Ottawa)
🏢 Everest Clinical Research
📍 Ottawa