Clinical Trial Assistant

1 settimana fa

Milano, Italia Dompè A tempo pieno

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.

**Long Description**
- 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; ecc
- Minimum one year the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in clinical research environment;

**Technical Expertise**
- 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.

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