Clinical Research jobs in Brazil
Explore 16 matching jobs.
Clinical Research Associate I, II, Senior
ICON plc
Posted: 10/20/2026Clinical Trial Manager
ICON plc
Posted: 10/16/2026Clinical Trial Manager
ICON plc
Posted: 10/16/2026Senior Clinical Trial Manager
ICON plc
Posted: 10/16/2026Country Regulatory Specialist, Clinical Research
Syneos Health
Posted: 10/15/2026Clinical Research Associate II
MSD
Posted: 10/15/2026Clinical Trial Manager
ICON plc
Posted: 10/14/2026Senior Clinical Trial Manager – LATAM
Precision For Medicine
Posted: 10/14/2026Senior Clinical Trial Manager – LATAM
Precision Medicine Group
Posted: 10/14/2026Clinical Research Associate I
ICON plc
Posted: 10/10/2026Clinical Research Associate
ICON plc
Posted: 10/6/2026Senior Clinical Trial Manager
ICON plc
Posted: 10/2/2026Clinical Research Associate II
CTI Clinical Trial and Consulting Services
Posted: 9/29/2026Clinical Research Development Analyst
LIBBS FARMACÊUTICA LTDA
Posted: 9/24/2026Senior Clinical Research Associate – Remote
Lifelancer
Posted: 9/18/2026Google Cloud Platform
Senior Clinical Trial Manager
ICON plc
Posted: 9/18/2026Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial monitoring, regulatory compliance, and site management, with a strong focus on data integrity and quality improvement. Proven ability to build relationships and influence stakeholders while managing multiple projects effectively.
Highest-signal resume keywords
Clinical Trial MonitoringRegulatory ComplianceSite ManagementData IntegrityStakeholder Management
About the role
Key responsibilities & impact- Monitor clinical trial sites for adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards
- Conduct site visits to assess site performance, resolve issues, and provide support
- Collaborate with cross-functional teams on timely and accurate data collection and reporting
- Provide training and guidance to site staff and other CRAs
- Build and maintain relationships with site personnel and stakeholders
- Lead clinical trial monitoring tasks with a focus on quality and continuous improvement
- Oversee and manage clinical trial activities according to protocol, regulations, and industry standards
Requirements
What you’ll need- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
- Proven ability to manage multiple sites and projects simultaneously
- Strong organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management
- Proficiency in relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management skills
- Ability to influence and drive compliance within a complex environment
- Willingness to travel as required (approximately 60%)
- Legal right to work in Brazil
Benefits
Comp & perks- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Clinical Trial ProcessesGood Clinical Practice (GCP)Site Performance AssessmentProject ManagementClinical Trial Software Proficiency
Soft Skills
Organizational SkillsProblem-Solving SkillsCommunication SkillsInterpersonal SkillsInfluencing Skills
Industry Keywords
Clinical Research AssociateHealthcareStudy ProtocolsCross-Functional CollaborationContinuous Improvement
