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 visits
• Provide support for site onboarding and informed consent preparations
• Compile and prepare packages for regulatory submissions




• Adapt documents to align with local regulations and standards
• Deliver expert regulatory guidance based on country specifics

Requirements:
• Senior CRA with high levels of autonomy
• Proven background in site selection and regulatory submissions
• Strong knowledge of local regulatory environments
• Experience with late-stage studies (phase II, III)
• Local language proficiency may be necessary

Utilize your skills in regulatory submissions and site management to make a significant impact in this international clinical research initiative.
#J-18808-Ljbffr

📌 Senior CRA for International Clinical Trials (Quebec City)
🏢 Bilinguallink
📍 Quebec City