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Clinical Research Associate II

Madrid, MD, esFull-time2026-09-30 → 2026-10-07

Core

Frontline communication with project stakeholders to ensure timelines, targets, and standards of clinical research projects across various therapeutic indications.

Builds

Clinical research projects

Domain

Life Sciences / Clinical Trials

Required skills

On-site monitoring, CRF review, source document verification, query resolution, site communication and management, regulatory document preparation, audit and inspection participation

Preferred skills

Feasibility research, vendor management, internal project team coordination

Technologies

MS Office

Responsibilities

Conduct and report SIV, RMV, COV onsite monitoring visits; Perform CRF review, source document verification and query resolution; Be responsible for site communication and management; Be a point of contact for in-house support services and vendors; Communicate with internal project teams regarding study progress; Participate in feasibility research; Support regulatory team in preparing documents for study submissions; Prepare and participate on audits and inspections