33 opportunités d'emploi pour trials en Belgique mises à jour aujourd'hui
offres d'emploi trouvées
· Page 1 / 2A clinical research organization is looking for an R Programming Lead in Zaventem, Belgium. The role focuses on developing and validating R packages for clinical trial analysis and building R-Shiny applications. Candidates should have strong R programming skills and experience in statistical program
Barrington JamesA leading consulting firm is seeking a GMP QA Consultant to maintain the integrity, quality, and compliance of clinical trials. Key responsibilities include conducting audits, reviewing documentation, tracking quality issues, and collaborating with clinical and regulatory teams. This role is pivotal
Grünenthal GroupA leading pharmaceutical company in Brussels is seeking a senior professional to lead the statistical direction for clinical evidence in Research & Development. This role requires a PhD in biostatistics and at least 10 years of experience in the pharmaceutical industry. The ideal candidate will have
Medpace, Inc.A clinical contract research organization is seeking a full-time Medical Physicist in Heverlee. The successful candidate will advise on dosimetry and nuclear imaging for clinical trials, ensuring compliance with safety guidelines. A PhD or Master’s degree with relevant experience is required, alongs
Proclinical StaffingA leading life sciences recruiter is seeking a Senior Clinical Site Manager or Senior Clinical Research Associate in Brussels. The candidate will manage clinical site operations, ensuring data integrity and compliance with regulations. Ideal candidates possess a bachelor's degree in Life Sciences, d
CluePointsA technology scale-up in Belgium is looking for a Machine Learning Engineer to transform clinical research through data-driven insights. The role involves developing machine learning models, leveraging deep learning platforms, and producing clean Python code. Candidates should have a Master's or PhD
MedpaceA clinical research organization in Belgium is seeking a Hematologist - Medical Director to provide medical and scientific leadership for clinical trials. The role involves managing trials, contributing expertise to reports, and ensuring safety protocols are followed. Ideal candidates must hold an M
IQVIAA leading clinical research organization is seeking a Local Study Associate Director to lead Local Study Teams in Belgium. This role involves managing clinical studies, ensuring compliance with international and local regulations, and coordinating site selection. Ideal candidates will have a Bachelo
MedpaceA clinical research organization is seeking a Hepatologist to provide medical leadership in clinical trials. The role involves managing studies, ensuring regulatory compliance, and collaborating with various departments. Candidates must have an M.D. degree with preferred experience in clinical resea
Barrington JamesA leading consulting firm is seeking a GMP QA Consultant in Brussels to ensure the integrity and compliance of clinical trials. You will conduct audits and monitor processes while collaborating with various teams to maintain high-quality standards. Ideal candidates will have experience in clinical t
A leading clinical contract research organization is seeking a Psychiatry Medical Director in Belgium. This role involves leading medical, scientific, and strategic efforts in clinical trials. Responsibilities include medical management, contributing to study reports, and ensuring adherence to proto
CapgeminiA leading technology consulting firm in Belgium is seeking an experienced Test Engineer specializing in pyrotechnical testing to manage critical trials in varied environments. You will prepare, conduct, and document tests, ensuring all standards of quality and safety. The role requires an electro-me
A leading technology consulting firm in Belgium is seeking an experienced Test Engineer specializing in pyrotechnical testing to manage critical trials in varied environments. You will prepare, conduct, and document tests, ensuring all standards of quality and safety. The role requires an electro-me
MedpaceA leading clinical research organization in Leuven is seeking a full-time Associate Director. In this role, you will oversee project management, prepare bids, and maintain customer relationships during clinical trials. The ideal candidate will have a Bachelor's degree and at least 7 years of experie
MedpaceA leading clinical research organization in Leuven is seeking a full-time Associate Director. In this role, you will oversee project management, prepare bids, and maintain customer relationships during clinical trials. The ideal candidate will have a Bachelor's degree and at least 7 years of experie
A leading technology consulting firm in Antwerp, Belgium, is seeking a Quality Assurance Leader to oversee compliance for clinical trial materials and diagnostics. The role involves leading a team of QA specialists, ensuring adherence to EU regulations, and driving continuous improvement in quality
Medpace, Inc.A clinical contract research organization is seeking a full-time Medical Physicist in Heverlee. The successful candidate will advise on dosimetry and nuclear imaging for clinical trials, ensuring compliance with safety guidelines. A PhD or Master’s degree with relevant experience is required, alongs
Proclinical StaffingA leading life sciences recruiter is seeking a Senior Clinical Site Manager or Senior Clinical Research Associate in Brussels. The candidate will manage clinical site operations, ensuring data integrity and compliance with regulations. Ideal candidates possess a bachelor's degree in Life Sciences, d
A technology scale-up in Belgium is looking for a Machine Learning Engineer to transform clinical research through data-driven insights. The role involves developing machine learning models, leveraging deep learning platforms, and producing clean Python code. Candidates should have a Master's or PhD
MedpaceA leading clinical contract research organization is looking for an Entry Level Regulatory Submissions Coordinator in Belgium. In this full-time position, you will play a crucial role in managing regulatory submissions to support clinical trial processes. Responsibilities include assisting in docume
26 000 € – 41 000 €par an
Confiance de l'estimation : Basse
Estimation basée sur les données du marché. Les salaires réels peuvent varier selon l'expérience, l'entreprise et la localisation.
Trouvez des offres de trials dans les principales villes de Belgique