First structure of institutional clinical research in France
Contacts: Dr Hendy Abdoul : email@example.com | Dr Pierre-Yves Ancel : firstname.lastname@example.org | Dr Caroline Elie : email@example.com | Pr Jean-Marc Tréluyer : firstname.lastname@example.org
Our structure takes in charge numerous missions and offers different tools to manage clinical research
Notre bilan d'activité de recherche en 2017. Nous couvrons l'ensemble des spécialités médicales avec une spécificité concernant les études mère-enfant et les maladies rares.
Study design and protocol writing, data base programming, monitoring, data management, statistical analysis
Modeling : population pharmacokinetic, PB/PK study, Bayesian approach, sequential approach, big data
Planning of teachings, course materials about clinical research, and registration processses
The Flesch index is an objective tool to evaluate the complexity of a text. Test the lisibility of the information letter dedicated to patients, or any other document
We propose a large offer of drug dosages for research purpose (HPLC, LC MSMS). Please download the appropriate asking form.
Clinical research in ethics related to research (information given to patients) and related to care (information given to adults and children, end-of-live in pediatrics)
In this section, you will find regulatory texts for clinical research and ublishing guidelines for scientific articles and activity reports
L'URC/CIC est basé sur 3 sites parisiens : Necker (Imagine), Cochin HUPC (Tarnier et Port-Royal)
Hospital Tarnier 89, rue d'Assas 75006 Paris France
Imagine 24 Bvd du Montparnasse 75014 Paris Cedex 14 France
Maternity Port Royal, 123 Bd de Port Royal 75014 Paris Cedex 14 France
The clinical research associate (CRA) is a key link between the promoter and the investigators. He is responsible for the initiation and follow-up of clinical studies, but also for the quality and authenticity of clinical data.
Clinical Research Associate
The clinical research technician participates in clinical data collection and in-site inclusions in collaboration with investigators and medical team of hospital. He also ensures that the clinical study is made in respect of SOPs and GCP, and that the quality control is optimal.
Clinical Research Technician
The project manager coordinates the implementation and development of clinical research projects, in accordance with regulatory requirements
The data manager is on the border between informatics and medicine. From crf design to final database extraction, he allows the relevance and quality of all the data related to a clinical trial.
The QA manager ensures that all activities are performed in accordance with GMP, company SOPs, and Health and Safety policies. He coordinates the QA management system, manages a self-inspection program to prepare to external audits, and ensures an internal formation program to maintain an up to date knowledge of all employees
The role of statistician is to applied statistical methods to medical and scientific research. He participates to data interpretation and is essential to publication of scientific research