Clinical Trials Start-Up Specialist

Fortrea in Belgium seeks a regulatory-focused professional to act as primary contact with investigative sites during study maintenance and startup, ensuring regulatory documents are collected and submissions are made on time. The role supports study management with senior staff and emphasizes adherence to ICH/GCP and local laws. The position requires a life...

IQVIA Brussels is seeking a contract specialist to support clinical trial contracting processes. You will develop investigator grants, craft contract language, and maintain templates, ensuring alignment with sponsor requirements and project plans. You will collaborate with sponsors and RSU regions to drive on-time delivery, provide expert contracting...

Role: Senior Clinical Project Specialist • Current Location: Brussels, Belgium Relevant Experience: 5+ YearsProfessional Summary: Experienced Clinical Project Specialist with over 5 years of experience supporting global clinical and medical device studies. Strong background in subject selection committee workflows, adjudication activities, vendor and...

Job Overview: Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within the timelines agreed with project management and Site...

Job Overview Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within the timelines agreed with project management and Site...

Job Overview: Primary contact with investigative sites during study maintenance and -when assigned-, site startup activities, with responsibility for collection of the required investigator and regulatory essential documents to ensure EC/IRB/Third body/Regulatory Authority submissions are made within the timelines agreed with project management and Site...

Job Description This position is part of a clinical research operations team supporting the management and coordination of independent review processes for clinical studies. The role is based in Belgium and offers a hybrid working arrangement, including one remote working day per week. ResponsibilitiesCoordinate and manage all aspects of independent review...

Job Title Clinical Application Specialist Hospital & Ambulatory Monitoring Job Description Share your knowledge by demonstrating the possibilities, explaining the functionality, training users, customizing systems and advising customers / end-users on the most optimal configuration. In this technical but commercially aware environment, you will contribute...

Are you highly organized, detail-oriented, and interested in contributing to clinical research? Do you have a first experience in clinical research ? Then this is a great opportunity for you ! We are looking for a Clinical Study Assistant to provide administrative and operational support to study teams throughout the lifecycle of clinical studies.Presence at...