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IQVIA Belgium is seeking a Clinical Research Associate to join our Site Management team. In this role you will monitor sites to ensure compliance with the study protocol, GCP and ICH guidelines, and sponsor requirements across multiple therapeutic areas.You will collaborate with sites to drive subject recruitment, administer study training, and manage study...

Alimentiv in Belgium seeks a Senior Clinical Research Associate to lead site monitoring and management for trials, ensuring compliance with ICH-GCP and study protocols. You will mentor junior CRAs and collaborate with cross-functional teams to drive data integrity and trial timelines.The role requires 40–60% travel, fluency in English, French and Dutch,...

Alimentiv is seeking an experienced CRA to independently perform and oversee all aspects of site monitoring, coordinating with sponsor sites and cross-functional teams in a high accountability environment. The role includes mentoring junior CRAs, conducting assessments and audits, and ensuring protocol and regulatory compliance in accordance with...

DPS Group Global in Belgium is seeking an MSAT Scientist to lead analytical method transfer and validation for commercial and pipeline biologics. You will combine hands-on lab work with data analysis, technical writing and cross-functional project support.This high-visibility role offers ownership of analytical projects, exposure to ICH, USP, Ph. Eur....

CTI Clinical Trial and Consulting Services seeks a skilled Clinical Research Associate to monitor sites and ensure regulatory compliance. You will serve as the main CTI contact for assigned study sites, performing PSV/SIV/IMV/COV visits within plan, while upholding ICH GCP standards.You will support start-up activities, collect essential documents, train...

Agomab Antwerp is seeking a Senior Clinical Trial Associate to provide high-quality administrative and operational support to the Clinical Operations Team. You will maintain study documentation, support TMF, ensure inspection readiness, and collaborate with CTMs, vendors and study teams in line with ICH-GCP and SOPs.The role requires strong organization,...

Worldwide Clinical Trials is seeking a Regulatory Affairs Specialist to support submissions across Belgium, France, and the Netherlands. In this remote role, you will partner with cross-functional teams to ensure timely, compliant regulatory submissions and maintain alignment with local and international requirements.The ideal candidate holds a bachelor’s...

Anacura is seeking a (Sr.) Scientist in Trace Analysis based in Belgium to design, develop and validate LC-MS methods for impurity investigations in pharma products. You will work on nitrosamines-focused analyses using LC-MS/MS and HRMS, ensuring compliance with ICH/FDA/EMA guidelines.You will join a dynamic CRO environment, interact with clients, and...

Technik Utrzymania Ruchu – Belgia (od 20 €/h) ABC Work to firma z wieloletnim doświadczeniem na rynku pracy. Pomogliśmy już setkom kandydatów w znalezieniu zatrudnienia. Legalność naszej działalności potwierdza wpis do Rejestru Podmiotów Prowadzących Agencje Zatrudnienia (KRAZ) pod numerem 12912. Zakres obowiązków: Realizacja planowych...

Eurofins PSS Insourcing Solutions® est une solution d'internalisation mondiale primée. Nous déployons notre équipe qualifiée directement sur le site du client, où elle gère les opérations de manière fluide et élimine les complexités. Nous garantissons un engagement stratégique et à long terme qui apporte de la valeur ajoutée directement sur le...

Jesteśmy generalnym wykonawcą budownictwa kubaturowego. Naszą specjalnością są budynki służby zdrowia, obiekty edukacyjne oraz szeroko pojęte działania inwestycyjne związane z podnoszeniem efektywności energetycznej budynków i ich termomodernizacją. Działamy w Polsce i zagranicą, przede wszystkim w Belgii, gdzie jesteśmy certyfikowanym...

argenx SE is seeking a Quality Compliance Lead to drive the effectiveness and compliance of the QMS, owning deviations, change controls, continuous improvement, and quality intelligence. You will partner with Quality, Regulatory, Manufacturing, and other functions to strengthen oversight and ensure inspection readiness.The role requires 7–10 years in a...

Functie omschrijvingAls MSAT Validation Scientist speel je een belangrijke rol in de ontwikkeling, validatie en overdracht van analytische methodes voor biologische geneesmiddelen binnen een biopharmaceutische omgeving in Geel. In deze functie combineer je wetenschappelijke expertise, labo-activiteiten en data-analyse om robuuste processen en betrouwbare...

Our client, a leading life sciences organization, is seeking an expert to lead comprehensive regulatory dossier assessments and file gap analyses. The project focuses on identifying compliance risks and developing scientific justifications to support regulatory submissions and health authority responses.Lead comprehensive gap analyses of regulatory dossiers...

BD is seeking a Senior Clinical Research Associate to support global medical device clinical studies. You will act as the primary contact for investigational sites, drive site performance, ensure regulatory compliance and maintain high data quality across studies.The role requires 5+ years in clinical research, 4+ years in site management, and travel up to...

IQVIA Belgium is seeking a Clinical Research Associate II for a sponsor-dedicated, home-based role in Belgium. You will perform site monitoring visits and manage recruitment plans while ensuring GCP and ICH regulatory adherence.The position offers ongoing training and cross-functional collaboration within IQVIA's extensive sponsor network. Ideal candidates...

AL Solutions is seeking a Senior Clinical Research Associate to lead set-up, execution and oversight of Phase I–IV trials across Belgium with occasional travel in the Benelux region. You will monitor studies to ensure compliance with ICH-GCP, EU and local regulations, study protocols, and SOPs, while mentoring junior team members.The role involves start-up...

Allucent is seeking a Clinical Research Associate (CRA) to independently monitor investigational sites, pro-actively detect issues, and ensure studies are conducted per protocol, SOPs, and GCP/ICH guidelines.You will lead monitoring activities, manage site relationships, and support startup activities, including contracting. Travel is required across Belgium...

Progressive zoekt een Projectingenieur HVAC voor een toonaangevende farmaceutische productieomgeving in Antwerpen. U ondersteunt de uitvoering van HVAC- en clean utility-projecten met focus op cleanrooms en GMP-omgevingen.Je werkt aan ontwerp, uitvoering en validatie van HVAC-systemen, stelt functionele specificaties op en bewaakt kwaliteitsnormen zoals GMP,...

Nasz klient jest renomowanym producentem wysokiej jakosci trumien, dostarczajacym swoje produkty z duzym naciskiem na rzemioslo, precyzje i jakosc wykonania. W zwiazku z ich rozwojem poszukujemy zmotywowanego **Operatora Maszyn** do dzialu stolarskiego.JobomschrijvingJako Operator Maszyn w dziale stolarskim bedziesz odpowiedzialny za róznorodne prace...