Remote Clinical Trials Admin & Documentation Specialist

Worldwide Clinical Trials is seeking a Clinical Trials Associate to support the project team across UK and Serbia with remote work. You will handle document control, site file preparation, and QA tracking while ensuring quality and timely delivery.

Applicants should have a degree or equivalent experience and at least one year in a related role, with strong English communication and proficiency in MS Office. This is a full-time remote role offering international opportunities.

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