PSI is a leading Contract Research Organization with 30 years in the industry offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

1. Core responsibilities:

1.1. Provides administrative support to the Study Startup department with processes critical for site activation.

1.2. Supports Feasibility department with feasibility research and site identification activities.

1.3. Maintains project-specific tracking systems and electronic Trial Master File (eTMF) throughout the study startup phase.

1. Open to 2027 graduate majored in Life Science, Pharmaceutical, Medical or related.

2. Prior experience in clinical research is a plus.

3. Workable English in oral, written and reading.

4. Proficiency in standard Microsoft Office applications.

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