Clinical Research Associate Ii

Psi CRO; Buenos Aires; On-site; ARS 900,000 - 1,300,000; Full time

Job summary

PSI CRO is seeking a Clinical Research Associate I in Buenos Aires to conduct and report onsite monitoring visits, support feasibility studies, and manage site communications. You will perform CRF review and source data verification while coordinating with internal teams and vendor services.

The ideal candidate has life sciences education, 1–2 years of independent on-site monitoring experience in Argentina, and fluency in English and Spanish, with strong MS Office skills and travel readiness.

Qualifications

• Degree in Life Sciences or equivalent
• 1–2 years of independent on-site monitoring experience in Argentina
• Experience in Phase II/III monitoring visits
• Fluent in English and Spanish
• Proficient with MS Office applications
• Ability to plan and work in a dynamic team
• Excellent communication, collaboration and problem-solving skills
• Willingness to travel

Responsibilities

• 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

Skills

Bilingual English & Spanish

MS Office

Communication

Collaboration

Problem solving

Travel ability

Education

Life Sciences degree

Tools

MS Office

Job description

We are the company that cares - for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

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.

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