Remote Clinical Trials Impact Lead

Valatam

Ciudad de Mendoza

Remote

ARS 92,241,000 - 138,361,000

Full time

5 days ago

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Benefits offered by this job

Annual leave

Health insurance

Retirement planning

LifeWorks EAP

Life insurance

Flexible benefits

Job summary

ICON is seeking a CRA II / Senior CRA to design and monitor clinical trials and ensure data integrity. You will conduct site visits, review data, and work with investigators to support study conduct while upholding ICH-GCP guidelines.

Ideal candidates hold a science-related degree and have at least 1.5 years of CRA experience, with strong organizational and communication skills. This role offers remote work options within Argentina and competitive benefits.

Qualifications

Bachelor's degree in a scientific or healthcare field is required.
+1.5 years of Clinical Research Associate experience.
Strong knowledge of clinical trial processes and ICH-GCP regulations.
Excellent organizational and communication skills.

Responsibilities

Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
Collaborating with investigators and site staff to facilitate smooth study conduct.
Performing data review and resolution of queries to maintain high-quality clinical data.
Contributing to the preparation and review of study documentation, including protocols and clinical study reports.