CTC

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