The coordination team is made up of:

• Medical coordinator : determines the CIC-P’s guidelines and politics, as much on the scientific scope as on the strategic one

• Medical assistant coordinator: provides support to the medical coordinator’s missions

• Clinical Research Coordinator (CRC) : ensures the supervision and management of the interdisciplinary investigation support team, under the responsibility of the medical coordinator. The CRC applies the guidelines determined by the medical coordinator in collaboration with / In relations to the RMQ (?) and ensures the connection with the different teams of the CIC-P

• Quality Assurance (QA) Specialist : defines the CIC-P’s quality policy in collaboration with the medical coordinator. The QA specialist maintains an efficient Quality Management System, consistent with the applicable regulations, and makes sure it is respected by all the CIC-P members.

• Administrative assistant : brings the necessary logistical support to ensure the proper functioning of the CIC-P

The investigation support team is made up of:

• Clinical Research Coordinator (CRC) : supervises and manages the nursing team

• Clinical Research nurses : ensure the care of the research participants; they execute the nursing care required by the research protocols and ensure the management of the biological samples. Their activity is interdisciplinary on all the CIC-P and University Hospital of Bordeaux fields.

The team is made up of:

• Methodologists : assist in the development of research projects and in the preparation of research documents under the responsibility of the methodologist in charge 

• Statisticians : develop statistical analyses, from the creation of the statistical analysis plan to the statistical report’s submission, under the responsibility of the statistician in charge.

• Data-managers : prepare the database for analysis and make sure of the integrity of the collected data, under the responsibility of the statistician in charge

• Database administrators : develop electronic Case Report Forms (eCRF) or database necessary for data entry in the case of paper CRFs, under the responsibility of the database administrator in charge.

A multidisciplinary team is created for each line of research of the CIC-P. The multidisciplinary teams are made up of:

• Head(s) of department: supervise the multidisciplinary team's activity and define the future directions of their department

• Head of Operations: coordinates the activity of the pharmacoepidemiology platform, under the responsibility of the Department’s Head 

• Clinical Research Coordinator (CRC): coordinates the activity of the department under the responsibility of the Department’s Head

• Clinical Research Associates (CRA): implement the protocol’s logistics, collect and enter clinical data, under the responsibility of the Principal Investigator and of the CRC or of the Heard of Operation if necessary