Clinical research organization seeks a Clinical Research Associate level 2 or Senior to design and analyze clinical trials, interpret medical data, and advance innovative treatments. The role involves monitoring activities, ensuring protocol compliance, and maintaining data integrity across trial sites in Spain.

Responsibilities

Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials

Ensure protocol compliance, data integrity, and patient safety throughout trial process

Collaborate with investigators and site staff to facilitate smooth study conduct

Perform data review and resolution of queries to maintain high-quality clinical data





Contribute to preparation and review of study documentation including protocols and reports

Requirements

Bachelor's degree in scientific or healthcare-related field

Minimum 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 fast-paced environment

Willingness to travel approximately 60% as required

Compensation: Competitive base salary and performance related incentives

📌 Senior Clinical Trial Administrator (Barcelona)
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📍 Barcelona