trial

Randstad Professional Life Sciences is op zoek naar een Clinical Research Associate (CRA) Als Clinical Research Associate ben je verantwoordelijk voor het beheer van klinische activiteiten op verschillende studielocaties voor de MedTech-groep. Je fungeert als de cruciale schakel tussen het interne klinische studieteam en het personeel op locatie. Je stelt...

ITG zoekt een studieverpleegkundige voor de Clinical Trial Site (CTS). Je combineert verpleegkunde met studiegerelateerde taken en werkt samen met studieartsen, verpleegkundigen, onderzoekers en ondersteunende diensten.Je voert paramedische taken uit zoals het meten van vitale parameters, toediening van studiemedicatie (inclusief vaccinaties) en afname...

Join Excelya, where Audacity, Care and Energy define who we are and how we work. We believe in creating ambitious solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.We are looking for a Clinical Trial Assistant to support the successful planning, execution and oversight of clinical trials across...

Randstad Professional Life Sciences is op zoek naar een Senior Clinical Research Associate (Senior CRA). In deze rol ben je de cruciale schakel tussen het klinische studieteam en de verschillende onderzoekslocaties binnen de MedTech-divisie van Johnson & Johnson. Je bent verantwoordelijk voor het volledige beheer en de monitoring van klinische trials op...

KPS Life is seeking a Clinical Study Specialist to support clinical trial teams and oversee documentation for internal and outsourced studies. The role collaborates with leadership, CROs, and vendors to ensure compliant, timely study execution.Responsibilities include preparing reports, coordinating meetings, maintaining TMF, and supporting site activation...

Excelya is seeking a Clinical Trial Assistant in Belgium to support planning, execution, and oversight of clinical trials across regional and site levels. You will help ensure regulatory compliance, maintain TMF readiness, and coordinate between internal teams, sites, and external stakeholders.The role demands strong organizational skills, experience with...

One2Treatis a forward-thinking partner for biopharmaceutical companies, dedicated to delivering transformative insights in clinical trial design, analysis, and market access evaluations to support holistic treatment decisions.One2Treatwas founded in July 2023 after four years of advanced Research and Software Development incubation within IDDI Group. Driven...

Droom je van een baan waarin je je kunt verdiepen in agronomie en landbouwkunde, met een internationale twist? Ben je analytisch, enthousiast en heb je goede beheersing van Nederlands en Engels? Als Field Trials Project Coördinatorzijn we op zoek naar iemand als jij! Lees verder om te ontdekken of deze kans bij je past. Standplaats Gent (Zwijnaarde),...

Senior Clinical Trial AssociateDepartment: Clinical DevelopmentEmployment Type: Permanent - Full TimeLocation: Agomab AntwerpDescriptionThe Senior Clinical Trial Associate (CTA) is providing high-quality administrative and operational support to the Clinical Operations Team. In this role, you will report to the Head of Clinical Operations. You will play a...

Thermo Fisher Scientific is seeking a Principal Scientist in Biostatistics to advance life-changing therapies through rigorous statistical work. You will work in a dynamic FSP environment, designing studies, developing protocols, and delivering final analyses with regulatory-grade quality.The role emphasizes collaboration with clients, adherence to ICH-GCP...

IQVIA Inc invites applications for a contracting specialist focusing on clinical trials. The role involves coordinating investigator grants, drafting contract language, and maintaining contracting tools to support multiple studies while ensuring regulatory compliance. You will collaborate with sponsors and RSU regions to deliver contracted scope on time,...

Medpace is seeking a Site Contract Manager to join our Clinical Operations team in Belgium. You will oversee end-to-end CTA processes for global, multi-site trials and develop study-specific CTA strategies with Sponsors and internal stakeholders. The role requires a Bachelor’s degree in a relevant field, CRO experience, and strong negotiation, leadership,...

Fortrea in Brussels seeks a Regulatory Submissions Specialist to support site activities, collect essential documents, and ensure timely regulatory submissions across EU countries. You will work with senior staff to compile, prepare, submit, and obtain approvals from IRB/IEC/Regulatory Authorities, liaise with vendors, and ensure compliance with ICH/GCP...

Fortrea in Belgium seeks a regulatory-focused professional to act as primary contact with investigative sites during study maintenance and startup, ensuring regulatory documents are collected and submissions are made on time. The role supports study management with senior staff and emphasizes adherence to ICH/GCP and local laws. The position requires a life...

Fortrea in Belgium seeks a regulatory-focused professional to act as primary contact with investigative sites during study maintenance and startup, ensuring regulatory documents are collected and submissions are made on time. The role supports study management with senior staff and emphasizes adherence to ICH/GCP and local laws.The position requires a life...

Job Function: R&D Operations Job Sub Function: Clinical Supply Operations Job Category: People Leader All Job Posting Locations: Beerse, Antwerp, Belgium Job Description: At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where...

One2Treatis a forward-thinking partner for biopharmaceutical companies, dedicated to delivering transformative insights in clinical trial design, analysis, and market access evaluations to support holistic treatment decisions.One2Treatwas founded in July 2023 after four years of advanced Research and Software Development incubation within IDDI Group.Driven...

PURPOSE OF THE FUNCTION:The Director, Trial Operations Excellence & Innovation Lead is responsible for shaping and executing the strategic transformation agenda for Clinical Trial Operations and ensuring organizational readiness in line with argenx vision.The role provides strategic leadership across Trial Operations and partner roles to identify,...

Medpace is seeking a Site Contract Manager to join our Clinical Operations team in Belgium. You will oversee end-to-end CTA processes for global, multi-site trials and develop study-specific CTA strategies with Sponsors and internal stakeholders.The role requires a Bachelor’s degree in a relevant field, CRO experience, and strong negotiation, leadership,...

EPM Scientific are partnering with a global Medical Device company to support clinical research in Electrophysiology. We seek a Clinical Research Specialist to execute and deliver company-sponsored trials across Europe, reporting to the Clinical R&D Manager.The role requires collaboration with investigators, sites, and vendors to ensure compliant, timely...