Coordinate all operational activities of clinical trials, from the study set up until the archiving together with the Clinical Project Manager:- Collaboration with the Clinical Project Managers during the preparation (writing and review) of all documents requested for the regulatory submissions (protocol, informed consent, synopsis)- Participation to selection of the sites/CROs (feasibility studies)- Participation to the set-up of clinical contracts according to the study protocol (review of bid grids)- Study budget follow up (invoices tracking, anticipation of budget overspending during the study and participation to the reconciliation process at the end of the study) - Preparation and follow up of submissions to Ethics Committees or International Review Boards - Support to submissions to the Competent Authorities- Supervision of CRAs (local & leaders) activities, starting from the CRA selections (interviews) and CRA Training- Close study follow up through reviews and approvals of monitoring reports: follow up & impact’s measurement of all deviations reported, identifying causes and suggesting solutions to the clinical team.- Follow up of patients’ safety during the study- Coordinate activities leading to the clinical study report finalization- Set up and update of the Trial Master File from study set up until archiving- Operational follow up: collaboration with all the departments involved in the clinical team and interface role with the CROs- Conduct of monitoring visits (initiation visits, interim visits and closure visits)- Participation to investigator meetings (in Germany & France)Study phases: Phase I, IIa and IIbTherapeutic areas: Dermatology (atopic dermatitis, acne, psoriasis, ichtyosis)Tested products: Topic and biologicGeographic areas: France, Germany, United States, Sweden, Canada, Austria, Poland, Israel, NetherlandOther: training supervisor experience (6 months)

Internship for 6 months followed by an apprenticeship for one year as Clinical Trial Administrator.Mission: To provide administrative support to the Clinical Project Manager from study set up until the archiving- Involvement in 2 studies (phase Ia and phase Ib)- Participation to submissions to Ethic Committees and support provided for submissions to Competent Authorities- Participation to the writing and reviewing of study documents- Set up and regular update of the Trial Master File- Participation to several monitoring visits- Study follow up through the monitoring tracking

Internship for 2 months in a Clinical Research Associate team as a first experience in the "operational" context of clinical trials (participation to subjects visits, review and update of the ISF, subject file preparation)