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Clinical Research Associate II (FSP - Sponsor dedicated)

What You Will Do

You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables and working collaboratively.

Key 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.

Your Profile

You will bring relevant clinical trial monitoring experience, along with the following qualifications and skills.

Required Qualifications And Experience

Bachelor's degree in a scientific or healthcare‑related field.

Minimum of 2 years of experience as a Clinical Research Associate.

Advanced English level.

In‑depth knowledge of clinical trial processes, regulations, and ICH‑GCP guidelines.

Strong organizational and communication skills, with attention to detail.

Ability to work independently and collaboratively in a fast‑paced environment.

Willingness to travel as required (approximately 60%).

What ICON Can Offer You

Our benefits are designed to be competitive within each country and are focused on well‑being and work‑life balance opportunities for you and your family.





Our Benefits Examples Include

Various annual leave entitlements.

A range of health insurance offerings to suit you and your family’s needs.

Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.

Global Employee Assistance Programme, Life Works, offering 24‑hour access to a integral network of over 80,000 independent specialized professionals who are there to support you and your family’s well‑being.

Life assurance.

Flexible country‑specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.

Equal Opportunity Statement

At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment.

All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.

Reasonable Accommodation

If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.

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Postúlate en Kit Empleo: kitempleo.com.ar/empleo/px93d

📌 Clinical Research Associate II (Buenos Aires)
🏢 Icon Strategic Solutions
📍 Buenos Aires