Clinical Trial Assistant Milano

Clinical Trial Assistant
Milano
Lombardia, Milano

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.