Clinical Trial Operations Specialist

IQVIA

Madrid

Presencial

EUR 25.000 - 36.000

Jornada completa

Hace 2 días

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Descripción de la vacante

IQVIA is seeking a Clinical Trials Assistant to support daily administrative activities with the Clinical Research Associates (CRAs) and Regulatory & Start-Up teams in Madrid. You will help maintain Trial Master File (TMF) records, ensure regulatory compliance, and assist with study documentation and archiving.

The role emphasizes collaboration, timely document handling, and accurate data flow across teams, with potential site-visit support after training.

Formación

Bachelor’s degree in life sciences or related field.
Minimum 1 year of experience as Clinical Trials Assistant.
Proficient in MS Word, Excel and PowerPoint.
Fluent in English and Spanish.
Strong time management and organizational skills.
Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Knowledge of GCP/ICH guidelines as provided in company training.
Knowledge of protocol requirements as provided in company training.

Responsabilidades

Assist CRAs and RSU with updating and maintaining TMF documents.
Support preparation, handling, distribution, filing, and archiving of clinical documentation.
Review study files for completeness.
Coordinate Clinical Trial Supplies and tracking information.
Track Case Report Forms (CRFs) and data flow.
Serve as central contact for project communications and docs.
May accompany CRAs on site visits after training.