Overview
In this evergreen role, you help drive clinical studies for a strategic sponsor in a highly collaborative, quality-focused environment. Based in Spain with remote options, you will monitor sites, ensure trials align with protocol and standards, and support study setup and regulatory activities. You may train junior staff and engage directly with clients, contributing to study progress and proposal work. This position offers ongoing opportunities to grow within a fast-paced, cross-border CRO setting.
Responsabilidades Monitor progress of clinical studies at investigative sites and ensure compliance with protocol, SOPs, ICH-GCP and applicable regulations
Coordinate study setup and monitoring activities (identify investigators, regulatory submissions, pre-study and initiation visits)
Support trials across various sizes and scopes and assist the study team
Train and mentor junior staff
Interact with clients, initiate payments,



and contribute to proposals and client presentations
Requisitos principales 4-year college degree or equivalent experience
CRA certificate
Minimum 5 years of CRA/SCRA experience in CRO, pharma, biotech, or medical device environments
Extensive experience in IVD, oncology, infectious diseases and gastrointestinal studies
Proven experience monitoring studies across multiple European countries (Germany, France, UK, Denmark)
Availability for domestic travel up to 50–60% (international travel for senior roles)
Fluency in Spanish and English; additional language skills are a plus
calm and thoughtful
detail-oriented
responsive and proactive
ICH-GCP knowledge and compliance
Study start-up activities experience
Regulatory submissions coordination

📌 Senior Clinical Research Associate (La Coruña)
🏢 Precision For Medicine
📍 La Coruña