CRA II, Clinical Trials Monitoring – Chile

ICON Strategic Solutions

Chile

Hybrid

CLP 18,000,000 - 24,000,000

Full time

2 days ago

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Benefits offered by this job

Various annual leave entitlements

Health insurance offerings

Competitive retirement planning

Global Employee Assistance Programme

Job summary

ICON Strategic Solutions is seeking a CRA II in Chile to design and analyse clinical trials, interpreting complex medical data to advance treatments. You will monitor sites, ensure protocol compliance and data integrity while collaborating with investigators and staff to support study conduct.

The role requires a Bachelor's in a scientific field and at least 2 years of CRA experience, with travel up to ~60%.

Qualifications

Bachelor's degree in a scientific or healthcare-related field.
Minimum of 2 years of experience as a Clinical Research Associate.
In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
Willingness to travel approximately 60%.

Responsibilities

Conduct 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.