Coordinator

He has the general scientific responsibility for the activities implemented by the CIC. He organizes and manages the CIC’s medical activities at a strategic level.

Associate physician

He leads the daily activities of the CIC. He prepares the presentation of projects to the Technical Committee and nominates the reporters and any external experts. He also carries out medical consultations.

Associate pharmacist

She leads the daily activities of the CIC. She participates in the management of experimental health products stored at the CIC and linked with the University Hospital pharmacy.

Research nurse

She assists the investigators in the practical conduct of the study, ensures the usual or specialized investigative techniques and biological samples. She implements and monitors biomedical research techniques in cooperation with the investigators. She ensures the usual or specialized laboratory techniques, and packages and stocks samples. She may also manage patient visit schedules and organize their transport.

Biostatician

Apart from his own research, the biostatician provides methodological advice, and participates also in drafting protocols, in the analysis of results and publications.

Data manager

Is responsible for the design of electronic observation notebooks and is also responsible for management and data processing

Clinical Research Associate (CRA)

Ensures that the clinical trial runs smoothly from implementation to completion, while guaranteeing the quality of data and compliance with the regulations in effect (administrative and logistical procedures, compliance with GCP, data collection and patient’s follow- up). The CRA provides logistical support and assistance to the investigators.

Manager

Is responsible for administrative management of the CIC, organizing meetings and receiving investigators and industrials. The manager is also responsible for organizing meetings and preparing the activity reports of the center, and is the contact person for all issues.

Administrative secretary

Is responsible for the physical and telephonic reception of patients and collaborators of the CIC. Their goal is to help the whole team in drafting reports, research projects and medical reports for patients treated at the center.

Quality manager

Implements and maintains the CIC’s quality approach in line with changes in its activity and the regulatory texts in force. They participate in drafting and revising the CIC’s own procedures under the responsibility of the coordinating doctor, and are responsible for training staff in these procedures

Health executive

Is the interface between the departments of the University Hospital and the CIC. In collaboration with the coordinator, the health executive draws up and implements the general project of the CIC in line with institutional policy, and is also responsible for non-medical staff.

Biobank Research technician

Is responsible for the reception, preparation, storage and transfer of biological samples collections as part of the CIC’s biobank. Transfers are made in consultation with the research department of the University Hospital.

Research engineer

Is responsible for all aspects of the Biothèque’s biological sample preparation and conservation activities, in particular those relating to the cellulotheque. It facilitates the implementation of translational research programs in conjunction with the site’s fundamental research units.

Hospital services officer

The hospital services officer is responsible for cleaning the premises of the CIC, crockery, bedrooms, laundry and staff uniforms, as well as heating and serving meals for research subjects.