Clinical Trial Assistant Milano

Clinical Trial Assistant
Milano
Lombardia, Milano

Direct message the job poster from Dompé

We are looking for a motivated and organized Clinical Trial Assistant to join our dynamic team in Milan.

The Clinical Trials Assistant (CTA) is responsible for project-supporting clinical drug research and development tasks.

The CTA will provide administrative and clinical trials assistance to the Project Managers and project team for start-up, active phase, and closeout activities for assigned clinical studies.

Key Responsibilities: To provide general administrative support to the Clinical Operations Department and assistance to Project Manager(s) and Project Director(s); To assist the Clinical Operations teams in completion of all required tasks to meet departmental and project goals; To support the Clinical Operations teams with ongoing conduct of studies; To be familiar with ICH GCP, appropriate regulations and relevant SOPs; To assist project teams with filing and/or finalization of study specific documentation and guidelines as appropriate; To set up, organize and maintain clinical study documentation (e. g. , Main Study Files, CRFs, etc. )

including preparation for internal/external audits, final reconciliation and archival; To assist in quality control audits of clinical study documentation (e. g. , Main Study Files, CRF Files, Monitoring Files, etc.

); To assist project teams with trial progress tracking; To contact CRO for specific requests (e. g. , enrollment updates, missing documentation, meeting arrangements, etc.

); To assist in the production of slides, overheads, etc. , as needed for project, departmental, sponsor and/or business development presentations.

Education: ? University degree – Medical Science; Biotechnology; etc.

Technical Expertise: Minimum one year in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in clinical research environment; Fluency in English and Italian – written and spoken; IT Knowledge: Microsoft Office (Word; Excel; PowerPoint) and Google Workspace (Gmail, Calendar, Meet, Chat, Drive, Docs, Sheets, Slides, Forms, Sites etc.

); Knowledge of medical terminology; Knowledge of ICH GCP (Good Clinical Practice); Good organizational skills, ability to manage multiple tasks and meticulous attention to detail; Good written and verbal communication skills; Ability to work in a team; Flexibility and versatility.

Seniority level Mid-Senior level

Employment type Full-time

Job function Other

Industries Pharmaceutical Manufacturing

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