Our Services:
Investigators
Our Services:
Investigators
In the following sections, you will find a list of ongoing clinical trials for each disease. For each trial, you will find its title, primary objective, and status (by clicking on each trial, you will be directed to the ClinicalTrials.gov page for that trial if you would like to learn more).
Useful documents and information
Good Clinical Practice (GCP) is a set of principles designed to ensure the safety of research participants as well as the quality and validity of the data generated. These are evolving guidelines. They specify the respective responsibilities of the sponsor and the investigator and require the implementation of appropriate controls.
All clinical research professionals must keep their good clinical practices up to date.
Here's a link to view them:
https://globalhealthtrainingcentre.tghn.org/les-bonnes-pratiques-cliniques-de-lich-e6-r2/
2025 Calendar
Technical Committee:
A committee comprising members of the CIC Steering Committee, as well as internal and external experts from various fields of activity, whose purpose is to evaluate projects to be carried out at the CIC based on criteria of scientific excellence, ethics, and logistical feasibility. All studies intended to be conducted at the CIC must be evaluated by the Technical Committee.
Methodology Committee:
A committee comprising members of the CIC Steering Committee, representatives of academic sponsors, methodologists, and statisticians, whose purpose is to advise you on setting up your projects (methodological, regulatory, and logistical advice, etc.).
These two committees meet five times a year. Upcoming dates:
September 15, 2025
November 17, 2025
January 19, 2026
March 30, 2026
June 8, 2026
Sample Investigator Resume Template
In the following sections, you will find a list of ongoing clinical trials for each disease. For each trial, you will find its title, primary objective, and status (by clicking on each trial, you will be directed to the ClinicalTrials.gov page for that trial if you would like to learn more).
Useful documents and information
Good Clinical Practice (GCP) is a set of principles designed to ensure the safety of research participants as well as the quality and validity of the data generated. These are evolving guidelines. They specify the respective responsibilities of the sponsor and the investigator and require the implementation of appropriate controls.
All clinical research professionals must keep their good clinical practices up to date.
Here's a link to view them:
https://globalhealthtrainingcentre.tghn.org/les-bonnes-pratiques-cliniques-de-lich-e6-r2/
2025 Calendar
Technical Committee:
A committee comprising members of the CIC Steering Committee, as well as internal and external experts from various fields of activity, whose purpose is to evaluate projects to be carried out at the CIC based on criteria of scientific excellence, ethics, and logistical feasibility. All studies intended to be conducted at the CIC must be evaluated by the Technical Committee.
Methodology Committee:
A committee comprising members of the CIC Steering Committee, representatives of academic sponsors, methodologists, and statisticians, whose purpose is to advise you on setting up your projects (methodological, regulatory, and logistical advice, etc.).
These two committees meet five times a year. Upcoming dates:
September 15, 2025
November 17, 2025
January 19, 2026
March 30, 2026
June 8, 2026
Sample Investigator Resume Template