Clinical Project Managers
An exciting opportunity to join an expanding team. Duties will include the overall project management of Belgian and international trials in a range of therapeutic areas.
Special interest: Cardiology, Oncology, Ophtalmology and CNS. Candidates will have a minimum of 2 years Project Management experience or equivalent.

Excellent knowledge of Dutch, French and English is essential.

Clinical Research

Brussels, Belgium

International Project Manager
We seek an international  project manager for our team in Brussels, Belgium. Duties will include the overall project management of  international clinical studies. This will include complete responsibility for planning, implementation, execution and controlling of these clinical trials with your multinational team. You have at least 3 -5 years of experience in clinical development as project manager, preferably for international studies.
As a life sciences graduate, pharmacist, medical doctor or similar, you also have a proven track record of study completion on schedule, within quality standards and within budget.  You have the ability to lead and manage international project teams , whilst maintaining quality standards throughout the entire study, as required by ICH GCP, FDA requirements as well as all relevant European and local regulations. Interactions with sponsors, investigational site staff and your international project team is routine for you. Your style of working is very structured but flexible and team oriented.
Together with your team building and management skills you are also fluent in English, Dutch and French, both spoken and written, and you have a good working knowledge of MS-Office applications. Travel requirement: approx. 30%

Clinical Research

Brussels, Belgium

Clinical Research Associate (CRA)
Duties will include investigator recruitment for national and international clinical studies and pre-study, initiation, routine and final monitoring visits to the investigational sites, coordination of all necessary regulatory documentation and the associated activities this requires. Willingness to travel, mainly within Europe, is a must.
Candidates should be life science graduates and you should have at least 2 years experience as a CRA and have a good understanding of ICH-GCP. You have the ability to work independently as well as communicating well with the project manager and team. You have excellent knowledge of English, Dutch and French both written and spoken. Experience with MS-Office applications is essential.

Clinical Research

Brussels, Belgium

Trainer
Our European Centre for Clinical Research Training (ECCRT), is looking for a trainer in the field of clinical research. To guarantee the high standard and quality training we require, both on a theoretical and practical level, you will have at least 4-5 years experience in clinical research as a CRA or project manager.
Your job will include the provision of interactive SOP training, internal and external training both public "in house" as well as tailored "on site" training and will cover all operational areas of clinical research at a variety of levels ranging from introductory to advanced target groups.
You have good IT knowledge, excellent communication skills and you are fluent in English, French and Dutch.

ECCRT

Brussels, Belgium