Clinical Research jobs in Brazil
Explore 17 matching jobs.
Clinical Research Associate
ICON plc
Posted: 10/21/2026Clinical 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 processes, ensuring protocol compliance and data integrity while maintaining patient safety. Strong organizational and communication skills facilitate effective collaboration with investigators and site staff.
Highest-signal resume keywords
Clinical Trial ProcessesICH-GCP GuidelinesData IntegrityClinical Research Associate ExperienceStudy Documentation Preparation
About the role
Key responsibilities & impact- Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
- Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
- Collaborate with investigators and site staff to facilitate smooth study conduct.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports.
- Work in a sponsor-dedicated model supported by ICON’s global expertise.
Requirements
What you’ll need- Bachelor's degree in a scientific or healthcare-related field.
- Minimum of 2 years of experience as a Clinical Research Associate.
- In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
- Strong organizational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast-paced environment.
- Willingness to travel as required (approximately 60%).
- Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
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
Protocol ComplianceData ReviewQuery ResolutionClinical Study ReportsSite QualificationMonitoring VisitsClose-Out Visits
Soft Skills
Organizational SkillsCommunication SkillsAttention to DetailIndependent WorkCollaborative Work
Industry Keywords
Clinical TrialsPatient SafetyScientific FieldHealthcare-Related FieldTravel Requirement
