With 27 years of experience, IDDI is seen as a valuable partner in the design, conduct and analysis of clinical trials. IDDI is a biostatistics and eClinical service provider offering trial design, centralized randomization (IWRS), clinical data management, statistical analyses including DMC support, and medical writing in the field of clinical research.
IDDI is headquartered in Belgium (Ottignies – Louvain-la-Neuve) with offices in the US. Over the last few years IDDI has achieved very good results.
To sustain and develop this growth, we are looking to fill the following positions for our Belgian office.
In collaboration with the Lead Clinical Data Manager, the Clinical Data Management EDC Specialist will be responsible for setting up the EDC system to collect clinical trials data. Your Responsibilities: Design the Electronic CRFs according to the data collection requirements of […]
In the position of Clinical Data Reviewer you will provide support to the Clinical Data Management team in managing specific data entry tasks, data review tasks and quality control activities. More specially, you will: Perform data review activities: Review the […]
The Clinical Project Manager is the key client contact for projects where IDDI is performing multiple tasks (randomization, clinical data management, biostatistics, and/or medical writing). As a Clinical Project Manager your key responsibilities will be to: Ensure optimal relationship with […]
