* Technical administrator
* Bilingual Dutch - English
* Familiar with the medical sector
For our client, an international growing organisation active in the medical sector, we are looking for several Trial Set-up Specialists to join the Trial Set-up which forms part of the Global Project Management Function. In Belgium, this (French) group is represented by more than 450 employees, spread over 4 entities.
As a Trial Set-up Specialist you will be working closely with the Project Manager to set-up the project accurately and on time.
This includes creation, maintenance and archiving divided into 4 different aspects.
First of all you will do the preparation of sponsor study documentation: Laboratory Specifications such as the services foreseen in a specific project based on the Trial Notification Form, the clinical study protocol and the study on the budget for and communication with the sponsor. Secondly you prepare the site study documentation: Central Laboratory manuals, the instruction leaflet (in English) of which you will also coordinate the translation, study specific requisition forms etc. Beside these 2 aspects you are responsible for the internal study documentation; for the local trial set-up and all departments with trial specific directives as established in agreement with the sponsor. Finally you will do the technical preparation of the study database which covers the follow-up on test code creation in Master Test Catalogue, initiation and finalisation of study-specific reference ranges and CTMS set-up configuration. You might also perform other tasks deemed necessary to assure good quality work.
Next to this position our client is also looking for two Trial Set-up Associates; this job implies the support and elaboration of various clinical studies.
We are looking for these three positions for an accurate administrator with a bachelor's degree preferable in medical or science related subjects and a minimum of 1-2 years of working experience in a medical or clinical environment. You have effective communication, organisation and time management skills and are flexible in dealing with problems such as scope and deadlines. You are strong analytical and have attention to detail skills. You speak fluently Dutch and English, notions of French is a bonus. You work easily with standard computer and office applications and technical databases e.g. CTMS (Clinical Trial Management System) database.
Our client offers a competitive salary. You will be able to work on interesting projects in a fast-growing environment with a professional team.
Are you interested in this vacancy as a Trial Setup Specialist? Surely contact Patty Cathelyn via 09/233.11.83 or send in your CV through the Hays HR website.