Location
Les Ulis, Essonne | France
Job description
At the international level, you will work with different international clinical operations leads and study team leaders who manage the studies.
Activities and responsibilities
- BE responsible for the management of study documentation in collaboration with the subcontractor in charge of the e TMF management and support the study team in the oversight of the subcontracted tasks
- Administrative support to the managers : slides, Excel files
- Organization of the trips, travel expenses
- Give support on the organization of different meetings by teams or in presential
- Responsible for meeting minutes as required by the study managers
- Give support in the welcoming/ onboarding of new comers
- TMF Archiving
- Any other tasks that could BE delegated by the other members of the team
- Back up of other assistants if needed
Profile
- Proven assistant training and experience
- At least 2 years of experience in clinical trials
- Knowledge about GCP (training ICH\_GCP in the last 2 years)
- Good skills in IT tools : Excel, power point
- Ability to manage multiple tasks in a dynamic environment with shifting priorities
- Very good communication skills
- Knowledge of English (writing and speaking)
- Very good Team spirit
Job tags
Salary
