If you are currently a CRA I looking forward to the next step of your career, this might be the right position for you
As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.
You will:
- Conduct and report all types of onsite monitoring visits
- Be involved in study startup and feasibility research
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Support regulatory team in preparing documents for study submissions





College/University degree in Life Sciences or an equivalent combination of education, training & experience
1 - 2 years of independent on-site monitoring experience in Argentina
Experience in all types of monitoring visits in Phase II / III
Full working proficiency in English and Spanish
Proficiency in MS Office applications
Ability to plan and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
Ability to travel
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

📌 Clinical Research Associate II (Buenos Aires)
🏢 Psicro
📍 Buenos Aires