Clinical studies

Manager: Sandra Dexpert

Mission

Set up and implement clinical research protocols within the laboratory.

Activities

  • Drafting of clinical research protocols
  • Preparation of applications for initial authorization to set up clinical research with ethics committees and decision-making bodies (CPP, ANSM, CNIL), as well as requests for amendments.
  • Drawing up agreements between Inrae and partner institutions (university hospitals, analysis laboratories)
  • Recruitment of patients or volunteers for studies
  • Collection of clinical and biological data
  • Processing of biological samples
  • Creation of databases
  • Biological assays
  • Statistical analysis of data

Skills

  • Good clinical practice
  • In-depth knowledge of regulations governing research involving the human person and the RGPD (General Data Protection Regulation)
  • Neuropsychiatric and psychological assessment interview
  • Biological assay techniques (Elisa, Transcriptomics, etc.)
  • Data management
  • Statistics

Equipment

Biological safety laboratory level 2 (L2) / Type II microbiological safety station