Clinical Trial Assistant position supporting site monitoring activities and regulatory compliance at a contract research organization. The role involves assisting with protocol adherence, documentation, and cross-functional coordination for clinical trial sites based in Madrid.
Responsibilities
- Assist with monitoring of clinical trial sites for protocol adherence and GCP compliance
- Support site management activities including documentation preparation and data entry
- Collaborate with cross-functional teams to resolve site-related issues and facilitate communication
- Maintain accurate records of site activities and contribute to monitoring report preparation




- Participate in training initiatives to develop clinical trial management knowledge and skills

Requirements
- Bachelor's degree in life sciences, healthcare administration, or clinical research
- Strong organizational skills and attention to detail with multitasking capability
- Excellent communication and interpersonal skills for team collaboration
- Basic knowledge of clinical trial processes and regulatory requirements preferred
- Willingness to travel approximately 25% as required
- Some clinical research or site management experience preferred but not mandatory

📌 CTC (España)
🏢 Icon
📍 España