Senior Clinical Research Associate
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Job Description
Senior Clinical Research Associate monitoring vaccine trials for ICON, a global clinical research organisation. Overseeing sites, compliance, data integrity, and trial execution in Buenos Aires remotely.
Responsibilities:
- Oversee and manage clinical trial activities according to protocol, regulatory requirements, and industry standards
- Lead clinical trial monitoring tasks requiring technical depth, with a focus 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 to ensure 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
Requirements:
- 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, with strong organizational and problem-solving skills
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools
- Open to work with vaccine protocols
- Willingness to travel as required (approximately 30%)
- Legal right to work in Argentina
Benefits:
- 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
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