Clinical Research Associate II

Psicro; Buenos Aires; Presencial; ARS 900.000 - 1.200.000; Jornada completa

Descripción de la vacante

PSI in Buenos Aires is seeking a Clinical Research Associate I to perform onsite monitoring for diverse clinical studies, ensuring high-quality standards across regulatory and data practices.

The role involves startup activities, feasibility research, CRF review, source data verification, and vendor coordination, with strong English and Spanish communication skills and proficiency in MS Office.

Formación

• 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

Responsabilidades

• 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

Conocimientos

On-site monitoring

Study startup & feasibility

CRF review & source data verification

Vendor communication

Team collaboration

MS Office proficiency

Educación

Life Sciences degree

Argentina work eligibility

Herramientas

MS Office

Descripción del empleo

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.