Clinical Research Associate II

PSI CRO AG · Buenos Aires, Argentina · full-time · Hybrid · September 18, 2026

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Posted September 18, 2026 · Read from PSI CRO
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Job Description

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

Qualifications

  • 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

Additional Information

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

Employer
PSI CRO AG
Location
Buenos Aires, Argentina · Hybrid
Contract
full-time