CRCM in Hepato-Gastroenterology - Nurse / Lab Technologist (M/F/X)

As a Clinical Research Coordinator in Hepato-Gastroenterology and for the Clinical Pharmacology Unit, you are in charge of the following responsibilities:

• You work within a multidisciplinary team and interact with the various stakeholders in clinical research, in compliance with Good Clinical Practice;
• You participate in the information and training of the various stakeholders involved in the research.
• You check the feasibility of the study in collaboration with the investigator and participate in the evaluation of study-related costs.
• You ensure that all steps of the protocol are respected and carried out within the required deadlines;
• You handle administrative management (document collection, completing CRFs, data verification, etc.) and are responsible for establishing billing related to research activities;
• You check the inclusion and exclusion criteria for patients.
• You ensure the smooth running of the clinical study for each patient in partnership with the other professionals involved in follow-up.
• You are responsible for handling the technical procedures required by the study.
• You perform the technical procedures necessary for the smooth running of the study (such as: blood and urine samples, ECGs, ABPM setup).
• You are responsible for reporting incidents, accidents, or omissions that occur. You ensure the monitoring and follow-up of side effects;
• You take an active part in patient information and education and participate in obtaining informed consent.
• You manage monitoring visits;
• You participate in investigator meetings, inspection visits, and audits;
• You participate in the closeout of the study, as well as managing and responding to various queries in order to close the Case Report Forms (CRFs).

📚 Required qualifications and experience:

• You hold a Bachelor's degree in Nursing or as a Laboratory Technologist (blood samples to be taken) 
• You have experience in a hospital environment  

🚀 Essential skills

• You have a perfect command of the Office Suite;
• You are fluent in French and have a decent level of English (minimum B1 level);
• You have good interpersonal skills and work well both independently and in an interdisciplinary manner;
• You have excellent work organization skills and a high sense of responsibility;
• You are endowed with a spirit of initiative and synthesis;
• You respect the corporate culture and professional secrecy. 

✨ Additional assets

• You have experience in clinical research or hold training in the field;
• Experience in clinical research or knowledge of Good Clinical Practice (GCP) and the guidelines, regulations, and standards governing clinical research is an asset;