Experteer Overview Senior CRA II to monitor and manage clinical sites for sponsor-dedicated studies, ensuring ICH-GCP, GPP, and protocol adherence across on-site and remote activities. You will support site qualification, initiation, monitoring, and close-out, while safeguarding data integrity and patient safety. You’ll collaborate with cross-functional teams, train junior staff, and contribute to real-world late-phase initiatives. This role offers impact through optimizing site performance and contributing to trial success in a fast-paced, global environment.Compensaciones / Incentivos
- Perform site qualification, initiation, interim monitoring, management and close-out visits (on-site or remote) ensuring regulatory and protocol compliance
- Assess site performance and staff, escalates issues, and develop action plans
- Verify informed consent processes and protect subject confidentiality
- Review source documents and CRFs, drive query resolution within timelines
- Oversee IP inventory, labeling, and handling per protocol
- Review ISF for accuracy and reconcile with TMF
- Document activities and support recruitment, retention, and status tracking
- Manage project scope, budgets,



and timelines; adapt to changing priorities
- Coordinate with study sites and lead meetings; train junior CRA staff
- Support audit readiness and participate in sponsor/vendor meetings
- Provide mentorship to junior staff; contribute to proposalsand defense meetings
- For RWLP, support site identification, chart abstraction, and regulatory updates
- Identify process improvements and develop site management strategy
- Contribute to Case Report Form design and edit checks
- Participate in bid defense meetings and RFP inputResponsabilidades
- Bachelor's degree or RN in related field or equivalent experience
- Knowledge of GCP/ICH and applicable regulatory requirements
- Proficient computer skills and quick to adopt new technologies
- Excellent communication, presentation, and interpersonal skills
- Moderate critical thinking ability
- Ability to travel up to 75% regularlyRequisitos principales
- career development and progression
- supportive line management
- technical and therapeutic area training
- peer recognition
- total rewards program
- inclusive culture

📌 Senior Clinical Research Associate Ii - Sponsor Dedicated. Madrid.
🏢 Syneos Health
📍 Madrid