Worldwide Clinical Trials seeks a Clinical Research Associate I for sites in Romania, Spain, or Poland. The role involves managing clinical trial data quality, regulatory documentation, and site operations while supporting a general CRO's mission to advance patient care through rigorous clinical research.
Responsibilities
- Monitor data quality from study sites and ensure timely, compliant data submissions with safety event follow-up
- Compile regulatory and ethical documentation including IRB approvals, informed consents, and lab certifications
- Maintain and update site documentation in the Trial Master File
- Conduct feasibility assessments and identify potential study sites as needed

Requirements
- Four-year degree in life sciences, or two-year degree plus one year clinical research experience
- Fluency in English, Romanian, and one additional language (German, French, Italian, Spanish, or Polish)
- Proficiency with Microsoft Office, CTMS, and EDC systems
- Strong written and oral communication skills
- Professional customer interaction and remote collaboration abilities

📌 In-House Clinical Research Associate I (España)
🏢 Worldwide Clinical Trials
📍 España