Remote CRA II - Clinical Trials (Spain, 60% Travel)

ICON Clinical Research

Barcelona

Remote

EUR 40,000 - 60,000

Full time

14 days+

Get a reply from this employer

Your resume and cover letter, tailored to exactly what they’re hiring for.

Get past ATS filters

Benefits offered by this job

Annual leave entitlements

Health insurance offerings

Retirement planning offerings

Global Employee Assistance Programme

Job summary

ICON Clinical Research in Spain seeks a Clinical Research Associate II to support home-based trial monitoring in a sponsor-dedicated model. You will design and monitor trials, interpret complex data, and contribute to advancing innovative treatments for patients worldwide.

Ideal candidates hold a Bachelor's degree in a scientific field, at least 2 years of CRA experience, and strong knowledge of ICH-GCP guidelines. Travel around 60% and collaboration with investigators are expected.

Qualifications

Bachelor's degree in a scientific or healthcare-related field.
Minimum of 2 years of experience as a Clinical Research Associate.
Knowledge of clinical trial processes, regulations, and ICH-GCP.
Strong organizational and communication skills.
Ability to work independently and in a fast-paced environment.
Willingness to travel approximately 60%.

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