clinical study

The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments, Briefing Books, Investigator’s Brochures (IBs) and IB updates, Biomarker Reports, and...

I'm working with an innovative biotechnology organisation that is expanding its data science and quantitative development capabilities. They are seeking an experienced Biomarker Statistics Lead to play a key role in shaping biomarker strategies across a growing development portfolio.Read on to find out what you will need to succeed in this position,...

Sunrise Group is building the future of sleep health by combining breakthrough technology with expert care. We started in 2015 with a straightforward idea: sleep diagnosis should happen in the comfort of your own home, not in a hospital. To make that possible, we created a first-of-its-kind chin sensor, carefully validated through clinical research, reviewed...

TiTANS Consulting seeks a Senior Business Analyst/Consultant to lead functional analysis, feasibility study, and migration planning for hospital ADT workflows to EPIC Prelude in a Belgian hospital context. The role requires deep knowledge of Belgian regulatory and interoperability frameworks (HL7/FHIR, eHealth, MyCareNet) and strong workshop facilitation...

Shape the future of evidence generation in Immunology and Rare DiseaseAre you passionate about using real-world data to answer critical scientific, regulatory, and healthcare questions? We are seeking an experienced Senior Real-World Evidence (RWE) Expert to lead the design and delivery of global evidence-generation programmes that directly influence...

The Sr Manager, Global Site Activation, Legal Liaison is responsible for providing expert operational support and guidance for clinical trial contracting activities when IQVIA Biotech is a contracting party. This role serves as a key point of contact for contracting matters, ensuring efficient issue resolution, consistency in contract practices, and...

The Sr Manager, Global Site Activation, Legal Liaison is responsible for providing expert operational support and guidance for clinical trial contracting activities when IQVIA Biotech is a contracting party. This role serves as a key point of contact for contracting matters, ensuring efficient issue resolution, consistency in contract practices, and...

RSU SpecialistLevel: Senior AssociateLocation: Belgium (Home-Based)About IQVIAIQVIA is a leading global provider of clinical research services, healthcare intelligence, and commercial insights to the life sciences industry. With more than 88,000 employees worldwide, we help accelerate the development and commercialization of innovative treatments that...

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to...

Shape the future of evidence generation in Immunology and Rare DiseaseMake sure to apply with all the requested information, as laid out in the job overview below.Are you passionate about using real-world data to answer critical scientific, regulatory, and healthcare questions? We are seeking an experienced Senior Real-World Evidence (RWE) Expert to lead the...

We are seeking a Principal Medical Writer to support full Clinical Study Report (CSR) writing for Phase 1 , protocol development, and preparation of regulatory modules (2.7.1/2.7.2) . This role requires strong writing skills and attention to detail to ensure high-quality, inspection-ready deliverables.Key Responsibilities:Ensure all deliverables are...

In vitro Biopharmaceutics Subject Matter Expert Akkodis is a global engineering and technology consulting company supporting organizations in the development, transformation and optimization of their products, systems, and operations. Our experts work across engineering, digital and software, Data & AI, manufacturing, and life sciences, contributing to...

In vitro Biopharmaceutics Subject Matter Expert Akkodis is a global engineering and technology consulting company supporting organizations in the development, transformation and optimization of their products, systems, and operations. Our experts work across engineering, digital and software, Data & AI, manufacturing, and life sciences, contributing to...

What we will accomplish together: Alsinova is looking on a regular basis for Medical Writers to join our consulting team for clients’ projects (from big pharma to small biotech) based in Belgium. Your mission (should you decide to accept it): Your potential challenges will be various, depending on the clients’ priorities. The list below gives you...

About the RoleAre you passionate about healthcare innovation and curious about how new ideas become real-world improvements for patients and healthcare professionals?The Clinical Study Unit (CSU) Belgium, part of Sanofi's North Europe MCO, is looking for a Local Innovation Trainee to join the team for a 6-month internship starting in September 2026.This is...

At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s most innovative companies unleash their potential. From autonomous cars to life-saving robots, our digital and software technology experts think outside the box as they provide unique R&D and...

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to...

We are looking for a Global Medical Evidence Strategy Lead who is strategic, collaborative and curious to join us in our Medical Communities team, based in our Headquarters office in Brussels, Belgium.About The RoleYou will lead the development and delivery of integrated medical evidence plans for designated medicines and indications. Working globally, you...

Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to...

Planet Pharma are currently partnered with an exciting global biotech and we are actively seeking an experienced Global Medical Safety Lead to join the business on a permanent basis. This is a hybrid role.To be considered for an interview, please make sure your application is full in line with the job specs as found below.Key Responsibilities:Act as the...