Phase II-III Monitoring CRA — Global CRO

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 dynamic team that supports global pharmaceutical and biotech companies in their clinical development efforts, contributing to innovative healthcare solutions.