Clinical Research Associate I, II, Senior

• 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

• 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

• 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