Clinical Trial Assistant

1 settimana fa


Milano, Italia IQVIA A tempo pieno

Job Overview
Perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.

Essential Functions
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines.
- Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures.
- Assist with periodic review of study files for completeness.
- Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
- Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.
- Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.

**Qualifications**:

- Master's Degree in Life Sciences
- 3 years administrative support experience.
- Equivalent combination of education, training and experience.
- Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
- Written and verbal communication skills including good command of English language.
- Effective time management and organizational skills.
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
- Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training.
- Knowledge of applicable protocol requirements as provided in company training.



  • Milano, Lombardia, Italia Evidilya A tempo pieno

    Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a:Clinical Trial Assistant (STAGE)to reinforce our Operational Team in Milan.Main Tasks:Collaborate and support the study team...


  • Milano, Italia Evidilya A tempo pieno

    Evidilya , the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a: Clinical Trial Assistant (STAGE) to reinforce our Operational Team in Milan. Main Tasks: Collaborate and support the study...


  • Milano, Italia CTI Clinical Trial Services, Inc A tempo pieno

    **Clinical Project Assistant / Coordinator for our Italian Team** **Job Purpose/Summary** - Responsible for supporting management efforts of Clinical Project Managers and Directors, ensuring timelines, and quality standards are being achieved. **What You’ll Do** - Support Clinical Project Manager / Director in completing management activities; supports...


  • Milano, Italia Evidilya A tempo pieno

    Evidilya , the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a: Clinical Trial Assistant (STAGE) to reinforce our Operational Team in Milan.Main Tasks: Collaborate and support the study...


  • Milano, Italia Evidilya A tempo pieno

    Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a:Clinical Trial Assistant (STAGE)to reinforce our Operational Team in Milan.Main Tasks:Collaborate and support the study team...


  • milano, Italia Evidilya A tempo pieno

    Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a:Clinical Trial Assistant (STAGE)to reinforce our Operational Team in Milan.Main Tasks:Collaborate and support the study team...


  • Via Milano, Italia Evidilya A tempo pieno

    Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a: Clinical Trial Assistant (STAGE) to reinforce our Operational Team in Milan. Main Tasks:Collaborate and support the study...


  • 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...


  • Via Milano, Italia Evidilya A tempo pieno

    Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is looking for a:Clinical Trial Assistant (STAGE)to reinforce our Operational Team in Milan.Main Tasks:Collaborate and support the study team...

  • Clinical Trial Assistant

    2 settimane fa


    Milano, Italia Aleph srl A tempo pieno

    Si ricerca un Clinical Trial Assistant (CTA) a tempo determinato con buone possibilità di passare a indeterminato entro un paio di anni. Possibilità di certificazione CRA in caso di requisiti fondamentali già soddisfatti. Si richiede un minimo di esperienza nella ricerca come CTA o study coordinator o ruoli analoghi. Sede di lavoro: Milano +...