Clinical Research Associate II based in Barcelona, Spain, supporting sponsor-dedicated clinical trial monitoring on a home-based model. The role involves site management, protocol compliance oversight, and data quality assurance across trial lifecycle.
Responsibilities
- Conduct site qualification, initiation, monitoring, and close-out visits
- Ensure protocol compliance, data integrity, and patient safety throughout trials
- Collaborate with investigators and site staff to facilitate study conduct
- Perform data review and resolve queries to maintain clinical data quality
- Contribute to preparation and review of study documentation and reports
Requirements
- Bachelor's degree in scientific or healthcare-related field
- Minimum 2 years of Clinical Research Associate experience
- 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
- Legal right to work in Spain
📌 CRA (España)
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📍 España