Senior Clinical Research Associate

• Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
• Lead clinical trial monitoring tasks requiring technical depth, focusing on quality and continuous improvement
• 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 support successful trial execution
• 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 to facilitate smooth trial operations

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• At least 5 years of experience in Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements
• 2 years of experience with Oncology protocols
• Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills
• Expertise in monitoring practices, data integrity, and site management
• Proficiency in relevant clinical trial software and tools
• Willingness to travel as required (approximately 60%)
• Advanced level of English
• Based in Buenos Aires
• Legal right to work in Argentina

• 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