Postúlate en Kit Empleo: kitempleo.cl/empleo/1dozvf

We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team at ICON plc.

What you will be doing

- 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.

Profile

- 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.
- Strong organisational and communication skills, with attention to detail.
- Ability to work independently and collaboratively in a fast‑paced environment.




- Ability to travel at least 60% of the time (international and domestic – fly and drive) and a valid driver’s license.

What ICON can offer you

- Competitive salary.
- Benefits designed to be competitive within each country and focused on well‑being and work‑life balance.
- Annual leave entitlements.
- Health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings.
- General Employee Assistance Programme with TELUS Health, offering 24‑hour access to a general network of over 80000 independent specialised professionals.
- Life assurance.
- Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

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Postúlate en Kit Empleo: kitempleo.cl/empleo/1dozvf

📌 Clinical Research Associate (Santiago)
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📍 Santiago