Clinical Research Associate II.

PSI; Buenos Aires; Presencial; ARS 6.696.000 - 8.928.000; Jornada completa

Descripción de la vacante

PSI is seeking a Clinical Research Associate I in Argentina to monitor sites and support study startup across Phase II/III trials. You will conduct on-site visits, review CRFs, verify source documents, and resolve queries while coordinating with internal teams and vendors.

Fluency in English and Spanish, plus MS Office proficiency, is required. Join PSI to advance your career in a dynamic, global clinical research environment.

Formación

• College/University degree in Life Sciences or equivalent.
• 1-2 years of independent on-site monitoring experience in Argentina.
• Experience in Phase II/III monitoring visits.
• Full working proficiency in English and Spanish.
• Proficiency in MS Office and ability to travel.

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

Documentation review

Communication

Teamwork

Educación

Life sciences degree

Herramientas

MS Office

Descripción del empleo

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.