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Content 2
  • member
  • team
  • department
  • center
  • program_project
  • nrc
  • whocc
  • project
  • software
  • tool
  • patent
  • Administrative Staff
  • Assistant Professor
  • Associate Professor
  • Clinical Research Assistant
  • Clinical Research Nurse
  • Clinician Researcher
  • Department Manager
  • Dual-education Student
  • Full Professor
  • Honorary Professor
  • Lab assistant
  • Master Student
  • Non-permanent Researcher
  • Nursing Staff
  • Permanent Researcher
  • Pharmacist
  • PhD Student
  • Physician
  • Post-doc
  • Prize
  • Project Manager
  • Research Associate
  • Research Engineer
  • Retired scientist
  • Technician
  • Undergraduate Student
  • Veterinary
  • Visiting Scientist
  • Deputy Director of Center
  • Deputy Director of Department
  • Deputy Director of National Reference Center
  • Deputy Head of Facility
  • Director of Center
  • Director of Department
  • Director of Institute
  • Director of National Reference Center
  • Group Leader
  • Head of Facility
  • Head of Operations
  • Head of Structure
  • Honorary President of the Departement
  • Labex Coordinator
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© William Beaucardet
Consultation au Centre médical de l'Institut Pasteur (CMIP).
Scientific Fields
Diseases
Organisms
Applications
Technique

About

Holder of a Master’s degree in Biological and Chemical Analysis at Paris Descartes University, then I completed with a Clinical Research’s formation, at Clinact Formation.
In 2014, I joined the UMS20 service unit headed by Professor Matthew Albert at the Department of Immunology at the Institut Pasteur. I took in charge of the operational follow-up of clinical studies based on research programs conducted by Inserm’s team in the Department of Immunology.
In 2018, I joined the clinical coordination team of the Translational Research Center (CRT-CC) headed by Nathalie Jolly. My mission is the operational follow-up of clinical studies managed by the CRT-CC with the clinical project managers.
I am in charge of the verification of the good progress of the clinical studies according to the Good clinical practice (GCP) during the visits of monitoring, the management of the e-CRF dedicated to the clinical projects (Software REDCap, Voozanoo), of the link between the various actors of the clinical research (promoter, investigators, researchers), the organization of the patient circuit and management of undesirable events.
These different experiences allowed me to acquire a know-how in Clinical Research in various scientific fields (immunology, hepatology, neurology, virology …) and to know the applicable regulation to research involving the human person.