Clinical Study Coordinator

PME namuroise - secteur médical Accent Jobs allie la flexibilité d'une agence d'intérim et la qualité d'une agence de sélection. Seuls des emplois pouvant déboucher sur un contrat fixe sont proposés. Pour ce faire, nous pouvons nous appuyer sur 700 collaborateurs passionnés qui aident chaque jour plus de 12 000 personnes à trouver un emploi. Comptant 230 agences, Accent Jobs constitue le plus grand réseau de la Belgique.

**Description**
Support for the clinical study investigator to comply with study protocol and related procedures. You will organize and schedule clinical research activities, carry out clinical data entry at the allocated study sites (both French and Dutch speaking), Set up and maintain a system for filing at the study site the ongoing clinical studies documentation pertaining to the Investigator's Site File and perform other support tasks necessary for the successful completion of clinical studies on the study site (s):Organize and set up a schedule of activities at the study site,Check the correct implementation of the different tasks required by the study protocol,Prepare biological samplesEnsure that biological samples are correctly stored and sent to the examination center,Ensure that the data necessary for the protocol are collected by the investigator (write files for data collection if necessary)Ensure the anonymity of the results,Enter clinical data in the Case Report Form (electronic or paper)Transmit the data to the management center, and answer any related queries about the dataSet up a filing and archiving system for clinical studiesVotre mission principale en tant que technicien & coordinateur d'études cliniques : le soutien au médecin investigateur d'étude clinique pour se conformer au protocole et procédures de l'étude.
- Vous organiserez et planifierez les activités de recherche clinique, effectuerez la saisie des données cliniques au sein des sites d'étude alloués (francophones et néerlandophones).
- Vous assurerez la mise en place et le maintien du système de classement de la documentation des études cliniques (Dossier du site de l'investigateur) et assurerez d'autres tâches de support

**Votre profil**
Required skills and qualities and expected level:Bachelor in a field related to health or life sciences or equivalentMastering of computer and office tools,AutonomousOrganization and attention to detail, ability to maintain detailed and accurate recordsGood sense of quality and ethicsWilling to travel nationally;Very good knowledge in English, French and Dutch (B2 level at least)Good interpersonal skills for interactions with investigators and / or their staff.you have a driver's license**Nous offrons