CRA II

ICON is a general healthcare intelligence and clinical research organisation
united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and
inclusion are at the heart of how we work and interact with each other,
customers, patients and suppliers.

We are currently seeking a Clinical Research Associate II to join our diverse
and dynamic team. As a Clinical Research Associate II at ICON, you will play a
pivotal role in designing and analyzing clinical trials, interpreting complex
medical data, and contributing to the advancement of innovative treatments and
therapies.

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

Your 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 organizational 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 should possess a valid driver’s license

* Good level of English language
LI-Remote

LI-LR1

Employment with ICON is contingent upon having the legal right to work in the
country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to
support your health

📌 CRA 2 (Madrid)
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📍 Madrid