Senior Vaccine CRA: Lead Clinical Trials & Site Oversight

ICON Strategic Solutions; Argentina; On-site; ARS 52,819,000 - 83,001,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

LifeWorks/Global EAP

Job summary

ICON Strategic Solutions in Argentina seeks an experienced Senior Clinical Research Associate to oversee monitoring activities and ensure trial conduct per protocol and GCP. You will travel ~30% to sites, manage multiple sites, and collaborate with cross-functional teams to support data quality and timeliness.

You will be responsible for site visits, issue resolution, training staff, and building strong site relationships while ensuring regulatory compliance and high standards.

Qualifications

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Associate with understanding of processes and regulatory requirements.
• Ability to manage multiple sites and projects with strong organizational skills.

Responsibilities

• Monitor clinical trial sites to ensure adherence to protocols, regulatory requirements, and GCP standards.
• Conduct site visits to assess performance, resolve issues, and support trial execution.
• Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
• Provide training and guidance to site staff to maintain high standards of conduct.
• Build and maintain strong relationships with site personnel and stakeholders.

Skills

Clinical trial monitoring

Site management

Data integrity

Regulatory compliance

Travel readiness

Education

Bachelor's degree in a relevant scientific discipline

Tools

Clinical trial software

Job description

ICON Strategic Solutions in Argentina seeks an experienced Senior Clinical Research Associate to oversee monitoring activities and ensure trial conduct per protocol and GCP. You will travel ~30% to sites, manage multiple sites, and collaborate with cross-functional teams to support data quality and timeliness.

You will be responsible for site visits, issue resolution, training staff, and building strong site relationships while ensuring regulatory compliance and high standards.