Pfizer seeks Senior Clinical Research Associates to manage investigator sites across clinical trials in Madrid. The role encompasses site monitoring, protocol compliance oversight, and quality assurance to support patient safety and regulatory standards throughout trial conduct and close-out.
Responsibilities
- Monitor assigned investigator sites from initiation through database lock, ensuring protocol compliance and quality delivery
- Serve as primary point of contact for investigator sites, coordinating with study teams and addressing operational and clinical issues
- Conduct site development, training and coaching to ensure staff compliance and patient safety
- Review and resolve data queries,



adverse events and protocol deviations within required timelines
- Mentor junior Clinical Research Associates and participate in process improvement initiatives

Requirements
- Clinical trial monitoring experience and GCP knowledge
- Site management and investigator relationship building experience
- Strong communication and problem-solving skills
- Ability to conduct onsite and remote monitoring activities
- Understanding of clinical protocols and therapeutic areas
- Experience with regulatory documentation and reporting

📌 Senior Clinical Research Associate I (España)
🏢 Pfizer
📍 España