Clinical Research Associate II or Sr
RemotePorto Alegre, Rio Grande do Sul, Brazil or Curitiba, Paraná, Brazil
Job Summary
Monitor clinical trial sites through on-site and remote visits, building strong relationships with investigators and site staff. Collaborate with cross-functional teams to meet project timelines while managing site-level study documentation, systems updates, and visit reports. Implement corrective actions when needed to maintain study integrity and ensure sites remain audit- and inspection-ready. This home-based role in São Paulo, Rio de Janeiro, Curitiba, or Porto Alegre requires fluency in English and Portuguese, a life sciences background, and one year of CRA experience. Candidates must be able to travel and hold a valid driver's license. Join a leading CRO committed to delivering life-changing medicines to patients through high-quality clinical trial execution.
Required Qualifications
- Detail-oriented
- Strong problem solver
- Highly communicative
- Collaborative
- Adaptable
- Motivated
- Accountable
- Able to work independently
- Positive
- Professional
- Comfortable supporting virtual and in-person teams
- Home-based role
- Residing in São Paulo City, Rio de Janeiro City, Curitiba, or Porto Alegre
- Fluent in English
- Fluent in Portuguese
- Bachelor's degree in life sciences, pharmacy, nursing, or related field
- Minimum of 1 year of CRA experience
- Able to travel
- Valid driver's license
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