Experteer Overview

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In this CRA I–II role, you will oversee clinical site activities to ensure regulatory and protocol compliance across the trial lifecycle. You collaborate with cross-functional teams to monitor data integrity and support site performance for successful study execution. You will work on real-world late-phase studies and sponsor-driven projects, contributing to audit readiness and risk-based monitoring. This is a hands-on, impact-focused position in a mission-driven, collaborative environment.

Compensaciones / Incentivos
• Perform site qualification, initiation, interim monitoring, and close-out visits (on-site or remote) with adherence to ICH-GCP and GPP
• Verify informed consent, protect subject confidentiality, and assess factors impacting safety and data integrity
• Conduct source data review, ensure accurate CRF entry, and drive query resolution within timelines
• Manage IP inventory and labeling, and verify IP dispensing per protocol
• Review ISF and TMF alignment, and ensure archival of essential documents
• Support recruitment/retention strategies and data tracking to monitor trial progress




• Prepare for and participate in investigator meetings and sponsor-facing events
• Provide guidance on audit readiness and support follow-up actions
• Maintain up-to-date knowledge of regulatory guidelines and SOPs
• Coordinate site activity within defined project scope, budgets, and timelines
• Train and supervise site staff as needed and liaise with sponsor/local teams
• Assist in Real World Late Phase study design and site identification
• Identify potential sites based on local treatment patterns and HCP networks

Responsabilidades
• Bachelor's degree or RN in a related field or equivalent
• Knowledge of xqbhyrx Good Clinical Practice/ICH Guidelines and regulatory requirements
• Strong computer skills and adaptability to new technologies
• Excellent communication, presentation, and interpersonal skills
• Ability to travel up to 75%
• Compliance with site access information requirements as needed for US sites
• Experience in clinical monitoring or site management is implied
• Proactive and able to adapt to changing priorities

Requisitos principales
• career development
• supportive line management
• total rewards program
• inclusive culture
• travel opportunities

📌 CRA I-II in Madrid. Sponsor dedicated.
🏢 Syneos Health
📍 Madrid