Urgent clinical research associate jobs in Brazil! ICON plc is hiring experienced CRAs for remote roles in São Paulo. Apply by December 29, 2025, for exciting opportunities in oncology, cardiology, and more therapeutic areas.
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About the Company
ICON plc is a world-leading healthcare intelligence and clinical research organization (CRO). Driven by innovation and excellence, ICON partners with pharmaceutical, biotechnology, and medical device companies to accelerate clinical development.
With a global presence and inclusive culture, ICON delivers full-service and functional outsourcing solutions across diverse therapeutic areas. The company fosters talent growth, diversity, and impactful contributions to advancing global healthcare.
Job Details
- Company Name: ICON plc
- Location: São Paulo, Brazil
- Work Type: Hybrid (Office or Home-based)
- Experience: Previous independent onsite monitoring experience as a Clinical Research Associate (CRA II or Senior CRA level)
- Qualification: Bachelor’s degree in a scientific or healthcare-related field
Job Description
ICON plc is seeking experienced Clinical Research Associates (CRA II and Senior CRA) to join its dynamic team in Brazil.
These remote/hybrid roles involve extensive site monitoring across full-service and sponsor-dedicated projects. Focus areas include oncology, cardiology, neurology, immunology, rare diseases, and hematology, with significant travel requirements.
Clinical Research Associate (CRA II / Senior CRA)
- Department: Clinical Operations
- Experience: Proven onsite monitoring experience (SIV, routine visits, close-out)
- Education/Qualification: Bachelor’s degree in scientific/healthcare field
- Key Requirements: In-depth ICH-GCP knowledge, advanced English proficiency, valid driver’s license, ability to travel 70% (domestic/international)
Skills/Qualifications
- Independent onsite monitoring expertise (SIV, routine, close-out visits)
- Strong knowledge of clinical trial processes and ICH-GCP guidelines
- Advanced English communication (reading, writing, speaking)
- Excellent organizational and attention-to-detail skills
- Ability to work independently in a fast-paced environment
- Valid driver’s license and willingness for extensive travel
- Collaborative mindset for working with investigators and site staff
Key Responsibilities
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance and patient safety
- Maintain data integrity through query resolution
- Collaborate with investigators and site personnel
- Perform data review and source data verification
- Contribute to study documentation and clinical reports
- Support smooth trial conduct across therapeutic areas
Benefits/Perks
- Competitive salary and performance rewards
- Generous annual leave entitlements
- Comprehensive health insurance options
- Retirement planning and life assurance
- Global Employee Assistance Programme (24/7 support)
- Flexible country-specific benefits (e.g., gym, childcare, travel)
- Inclusive culture with diversity and belonging focus
How to Apply
Apply immediately through the official ICON plc careers portal before the deadline of December 29, 2025. Search for requisition ID JR140322 or visit the ICON careers site directly.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the ICON Plc Career page.
For additional clinical research and CRA job opportunities worldwide, explore Pharma Recruiter. Don’t miss this limited-time opportunity – submit your application today!
Why You Should Join
ICON plc offers a diverse, inclusive environment where high performance is rewarded and talent thrives.
Join a global leader shaping the future of clinical development while enjoying work-life balance, professional growth, and meaningful impact on innovative therapies.
Benefit from supportive policies, global opportunities, and a culture committed to well-being, inclusion, and excellence in healthcare advancement.
FAQs
What experience is required for the Clinical Research Associate role at ICON?
Candidates must have previous independent onsite monitoring experience as a CRA, including SIV, routine, and close-out visits.
Is this CRA position fully remote?
The role is hybrid (office or home-based) in São Paulo, Brazil, with at least 70% travel required (domestic and international).
When is the application deadline for this position?
Applications close on December 29, 2025. Submit promptly via the ICON careers portal (requisition JR140322).
What therapeutic areas does this CRA role cover?
Positions involve oncology, cardiology, neurology, immunology, rare diseases, and hematology in full-service or sponsor-dedicated models.