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

📌 CRA 2 o SCRA (España)
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📍 España