Author-coordinator Clinical guidelines - Brussels

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. · ...

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, 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 ...

+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 ...

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

Under the direct supervision of a clinical services shift leader, the Clinical Research Generalist provides the upfront delivery of clinical research care to participants within the Brussels Clinical Research Unit (CRU). Their core duties include performing hands-on data collecti ...

· Clinical Research Associate Belgique · Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realit ...

Under the direct supervision of a clinical services shift leader, the Clinical Research Generalist provides the upfront delivery of clinical research care to participants within the Brussels Clinical Research Unit (CRU). Their core duties include performing hands-on data collecti ...

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. · ...

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 ...

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 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 ...

Regular · Exempt · GENERAL DESCRIPTION: · Evaluates utilization in clinical records and hospital facilities concurrently and retrospectively. Identifies and refers to other clinical departments (Case management, condition management, among others) cases for the management of trea ...

Job Overview · Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include ...

This position will support and observe clinical site monitoring services both inhouse and in the field whilst developing CRA skills and knowledge. · ...

Work Schedule · Standard (Mon-Fri) · Environmental Conditions · Office · As part of the Thermo Fisher Scientific team, you'll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life every single day to enable ou ...

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. · ...