Clinical Research Coordinator (Contractor, Onsite)

RapidTrials is seeking an experienced Clinical Research Coordinator to provide immediate onsite support for a pediatric rare disease clinical trial at a research site in Spain. The primary near-term focus of this role is to help the site begin and accelerate patient pre-screening and screening activities.

The contractor will work under the direction and delegation of the Principal Investigator (PI) and designated site study team. Responsibilities may include medical record review, identification of potentially eligible participants, screening coordination, study documentation, data entry, participant and family communication, and coordination of protocol-required assessments. Final eligibility decisions, medical judgment, informed consent oversight, and other investigator responsibilities remain with the PI and appropriately delegated site personnel.

Type of Position: Contract, Onsite

Study: Pediatric Rare Disease Clinical Trial

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