Remote Senior Clinical Research Associate (CRA II)

Maurices; Buenos Aires; Remote; ARS 1,800,000 - 2,800,000; Full time

Benefits offered by this job

Health insurance

Life insurance

Flexible benefits

Job summary

ICON is seeking a CRA II / Senior CRA to design and analyse clinical trials, interpreting complex medical data to advance therapies. You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety across the trial lifecycle.

You will collaborate with investigators and site staff, perform data review, resolve queries, and contribute to study documentation.

Qualifications

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 1.5 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; detail-oriented.

Responsibilities

• 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 study conduct.
• Perform data review and resolution of queries to maintain high-quality data.
• Contribute to the preparation and review of study documentation, including protocols and reports.

Skills

Clinical trial monitoring

Data analysis

Regulatory knowledge

ICH-GCP familiarity

Education

Bachelor's degree in science/healthcare

Job description

ICON is seeking a CRA II / Senior CRA to design and analyse clinical trials, interpreting complex medical data to advance therapies. You will conduct site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety across the trial lifecycle.

You will collaborate with investigators and site staff, perform data review, resolve queries, and contribute to study documentation.