Clinical Research Associate II
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About the role
Remote, full-time Clinical Research Associate II role with PSI in São Paulo. Responsibilities include onsite monitoring visits, study startup and feasibility work, CRF review, source document verification, query resolution, site management, team communication, vendor coordination, and regulatory submission support. Requires a college/university degree in Life Sciences or an equivalent combination of education, training and experience, independent on-site monitoring experience in Argentina, Phase II/III monitoring experience, English and Spanish proficiency, and travel ability.
Key requirements
- • College/University degree in Life Sciences or an equivalent combination of education, training & experience
- • Required skills: Independent on-site monitoring experience in Argentina, Experience in all types of monitoring visits in Phase II / III, Proficiency in MS Office applications, 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: Remote
- • Posted: Nov 4, 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: São Paulo, SP, Brazil
Employment type: Full-time
Workplace type: Remote
Company Description
PSI is a leading Contract Research Organization with more than 25 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.
Job Description
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
- Independent on-site monitoring experience Argentina
- Experience in all types of monitoring visits in Phase II / III
- Experience in Oncology is preferred
- 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: Nov 5, 2026