Clinical Research Associate II
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About the role
PSI seeks a Clinical Research Associate II in Buenos Aires to conduct onsite monitoring visits, support study startup and feasibility, review CRFs and source documents, resolve queries, manage site communication, coordinate with project teams and vendors, and support regulatory submissions. The role requires a Life Sciences degree or equivalent education, training and experience, 1–2 years of independent onsite monitoring experience in Argentina, Phase II/III monitoring experience, English and Spanish proficiency, and travel availability.
Key requirements
- • College/University degree in Life Sciences or an equivalent combination of education, training & experience
- • At least 1 year of relevant experience
- • Required skills: Independent on-site monitoring experience in Argentina, Experience in all types of monitoring visits in Phase II / III, MS Office proficiency, Ability to plan and work in a dynamic team environment, Communication skills, Collaboration skills, Problem-solving skills, Ability to travel
- • Required languages: English, Spanish
Opportunity details
- • Workplace: On Site
- • Posted: Sep 18, 2026
- • Original advert language: English
Full vacancy
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See original vacancy ↗Employer’s role description
Job title: Clinical Research Associate II
Location: Buenos Aires, Buenos Aires, Argentina
Employment type: Full-time
Company 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.
Verification
- ✓ Employer verification
- ✓ Original posting located
- Last verified: Sep 29, 2026