Author-coordinator Clinical guidelines - Brussels

The Author-coordinator of Clinical guidelines will coordinate the development and maintenance of content quality for MSF Clinical Guidelines. · ...

Médecins Sans Frontières (MSF) is an international medical humanitarian organisation that delivers emergency aid to people affected by armed conflict, epidemics, healthcare exclusion and natural disasters. · ...

· medical doctor · ...

Médecins Sans Frontières (MSF) is an international, independent medical humanitarian organisation that delivers emergency aid to people affected by armed conflict. The Author-coordinator coordinates the development and maintenance of content quality of MSF Clinical Guidelines. · ...

DICE is a CRO specialized in Biometrics and more specifically in project initiation, data management, statistics & medical writing.We differentiate by our highly skilled staff, bio statistical knowledge and drive to deliver the best quality to our customers. · As a Bio-statistici ...

DICE is a CRO specialized in Biometrics and more specifically in project initiation, data management, statistics & medical writing. We are seeking to employ a Senior Biostatistician. · ...

We seek a Scientific Coordinator CRA Inhouse in Brussels for an office-based position. As Inhouse · CRA you will support clinical project teams in planning and execution of clinical trials. · Liaise with internal study team and study sites to ensure timely start-up · and proper ...

The Clinical Research Generalist provides clinical research care to participants within the Brussels Clinical Research Unit (CRU). · ...

+Join Fortrea as a Clinical Research Associate and play a key role in advancing impactful clinical research. · +You will conduct all aspects of study site monitoring, including routine visits, initiation, and close‑out activities. · You will oversee site management activities in ...

Under direct supervision of clinical services shift leader, Clinical Research Generalist delivers upfront delivery of clinical research care to participants within Brussels Clinical Research Unit(CRU). · ...

We are looking for an additional Clinical Research Associate to support our team in Belgium. · The successful candidate will perform site qualification, site initiation, interim monitoring, site management activities and close-out visits ensuring regulatory compliance. They will ...

We are looking for a Clinical Research Associate to join our team in Belgium. As a CRA, you will oversee and ensure the integrity of clinical research studies by monitoring data and processes from a centralized location. · ...

This role involves coordinating study activities, ensuring data integrity, maintaining regulatory compliance, · supporting investigators. · ...

TFS HealthScience is a leading global mid-size Contract Research Organization (CRO) that partners with biotechnology and pharmaceutical companies throughout their entire clinical development journey. · ...

We are looking for an additional Clinical Research Associate to support our team in Belgium. · The monitoring visits will mainly be in Wallonia.We are responsible for overseeing and ensuring the integrity of clinical research studies by monitoring data and processes from a centra ...

Are you a detail-oriented proactive administrator with a passion for supporting clinical research Join our dynamic Clinical R&D team as Clinical Study Administrator and play a vital role in the success of clinical trials. · ...

We are looking for a detail-oriented, proactive administrator to support clinical research as a Clinical Study Administrator. You will support project managers and clinical study staff in ensuring the completeness, accuracy, and proper management of essential study documentation. ...

This role will support and observe clinical site monitoring services both inhouse and in the field whilst developing CRA skills and knowledge. · A clinical research associate (CRA) plays a key role supporting clinical trials by ensuring compliance with protocols, SOPs and regulat ...

The Clinical Research Associate works under the hierarchical supervision of: Head of Clinical Operations Department. The CRA is responsible for site monitoring ensuring that clinical studies are conducted, recorded, and reported in accordance with the protocol, Good Clinical Prac ...

The Clinical Research Associate works under the hierarchical supervision of: Head of Clinical Operations Department. · Main responsibilities / Major Activities · The CRA is responsible for site monitoring ensuring that clinical studies are conducted, · recorded, and reported in a ...