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Job Description & How to Apply Below
Become a crucial part of ethica CRO Inc. as a Clinical Project Associate. This remote position focuses on supporting clinical teams in planning, implementing, and reporting vital clinical studies.
We are seeking two motivated Clinical Project Associates to enhance our clinical research efforts at ethica CRO Inc. This role requires a strong understanding of ICH-GCP guidelines and at least two years' experience in a clinical research capacity. Key skills include assisting with trial management, site communication, and document preparation, all while meeting deadlines and maintaining high standards.
Key Responsibilities:
• Support Clinical Project Managers and Clinical Research Associates
• Track and ensure key clinical study milestones
• Assist with Trial Master File and Clinical Trial Management System
• Manage site database and contact information
• Prepare study documentation and forms
Requirements:
• University degree in health-related discipline
• At least 2 years in Clinical Research
• Experience in a CRO environment preferred
• Bilingual in English and French
• Strong computer skills in MS Office
Contribute to pioneering clinical research with effective communication, project management, and teamwork.
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Position Requirements
10+ Years
work experience
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