An established industry player is seeking a dedicated Clinical Research Associate to monitor clinical studies in phases II-III. This role involves ensuring compliance with Good Clinical Practices and overseeing site initiation and close-out processes. The ideal candidate will have a Bachelor's degree in life sciences and at least one year of monitoring experience within a CRO or pharmaceutical environment. Join a energetic team that supports global pharmaceutical and biotech companies in their clinical development efforts, contributing to innovative healthcare solutions.
📌 Clinical Research Associate For Regulatory Compliant Trials (Le Plateau-Mont-Royal)
🏢 Resourcing Life Science
📍 Le Plateau-Mont-Royal
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