Take charge of site selection in an international randomized clinical trial as a Senior Clinical Research Associate. This position emphasizes autonomy, regulatory knowledge, and site management.We are seeking an experienced Senior CRA to facilitate the launch of a pivotal clinical trial across Europe, Canada, and the United States. Your role will include site selection, supporting onboarding processes, and ensuring proper regulatory submissions and adaptations.



You will navigate local requirements with precision and expertise.Key Responsibilities:Lead site selection efforts and conduct essential in office visitsProvide support for site onboarding and informed consent preparationsCompile and prepare packages for regulatory submissionsAdapt documents to align with local regulations and standardsDeliver expert regulatory guidance based on country specificsRequirements:Senior CRA with high levels of autonomyProven background in site selection and regulatory submissionsStrong knowledge of local regulatory environmentsExperience with late-stage studies (phase II, III)Local language proficiency may be necessaryUtilize your skills in regulatory submissions and site management to make a significant impact in this international clinical research initiative.

📌 Senior Cra For International Clinical Trials (Saguenay)
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📍 Saguenay