Senior Clinical Research Associate

Overview

Senior CRAs in Spain join an evergreen talent pipeline to support a strategic sponsor in a collaborative, quality-driven environment. You will monitor studies, ensure compliant conduct, and work across cross-functional teams from site setup to study closeout. The role offers home-based flexibility and opportunities to mentor junior staff and engage directly with clients. This is a high-impact position focused on delivering quality clinical data and supporting complex, multi-country trials.

Responsabilidades

• Monitor progress of clinical studies at investigative sites to ensure adherence to protocol, SOPs, ICH-GCP, and regulations
• Coordinate study setup and monitoring activities: identify investigators, regulatory submissions, pre-study and initiation visits
• Support trials of varying scope within a CRO/pharma environment, including larger studies
• Train and mentor junior staff members
• Interact with clients, initiate payments, and contribute to proposal development and client presentations

• Minimum 5 years of CRA/ SCR A experience in CRO, pharmaceutical, biotechnology, or medical device environment
• Experience in IVD, oncology, infectious diseases, and gastrointestinal studies
• Proven multi-country monitoring experience in Europe (Germany, France, UK, Denmark)
• Domestic travel up to 50–60% (international travel may be required for some roles)
• Fluency in Spanish and English; additional languages a plus
• Holder of CRA certificate
• 4-year college degree or equivalent

• calm and thoughtful under pressure
• strong preparation and proactive planning
• attention to detail
• ICH-GCP compliance
• regulatory submissions coordination
• site monitoring and study management