Vacatures clinical in Utrecht

Clinical Trial AssociateAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit...

Clinical Research Principal Investigator A new and exciting opportunity has now arising for a Principal Investigator to join us at an exciting period of growth. As part of our continued expansion, we are seeking an experienced Principal Investigators based in the Netherlands to work with us across a range of therapeutic areas. This is a flexible...

UMC Utrecht zoekt een radioloog voor samenwerking met radiologie en nucleaire geneeskunde, inclusief mogelijkheden met WKZ en PMC en non-vasculaire interventies. Betrokken bij onderwijs, onderzoek en opleidingsactiviteiten en MDO-besprekingen met regio/patiënten.Je sluit aan bij een grote groep radiologen en nucleaire geneeskundigen en werkt mee aan...

At Genmab, we are dedicated to building extra[not]ordinary® futures, together, by developing antibody products and groundbreaking, knock-your-socks-off KYSO antibody medicines® that change lives and the future of cancer treatment and serious diseases. We strive to create, champion and maintain a global workplace where individuals’ unique contributions...

Als Clinical Study Researcher binnen het Early Life Clinical Evidence team ben je verantwoordelijk voor het opzetten, begeleiden en interpreteren van klinische studies gericht op zuigelingen en jonge kinderen. Je vertaalt zakelijke vragen naar wetenschappelijke hypothesen en kiest fit-for-purpose methodologieën, van interventietrials tot...

A leading biotechnology company based in Utrecht is looking for an Associate Director to lead statistical strategies for clinical development. The candidate should have a Master's or PhD in a statistical discipline along with over 8 years of experience in statistical analysis and drug development. Key responsibilities include engaging with regulatory...

A biotechnology firm in Utrecht is seeking a Regulatory Affairs Manager to support regulatory submissions and compliance activities for clinical studies. The ideal candidate will have at least 3 years of experience in regulatory affairs, particularly within the pharma or biotech industry, and must be knowledgeable about regulatory requirements and clinical...

Azza HealthCare Agency is seeking a Director, EU/ROW Regulatory Lead to join the Global Regulatory Affairs team. The role involves representing Regulatory Affairs in Clinical Trial Teams, overseeing trial submissions and collaborating with CROs and internal stakeholders to ensure regulatory progress across EU/ROW markets.The candidate will lead regulatory...

Clinical Trial AssociateAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit...

Clinical Trial ManagementAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit...

Clinical Research AssociateICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.As...

Company DescriptionPSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.Job DescriptionAs a Senior CRA, you will work on the frontline of...

Senior Clinical Research Associate - Area EindhovenICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers,...

We are the people who give possibilities purposeBD is one of the largest global medical technology companies in the world. Advancing the world of health™ is our Purpose, and it’s no small feat. It takes the imagination and passion of all of us—from design and engineering to the manufacturing and marketing of our billions of MedTech products per...

OverviewCo-Founder & Director of Operations at TargED Biopharmaceuticals. TargED is a biotechnology company in Utrecht, the Netherlands, developing first-in-class biological drugs to improve treatment of thrombosis. Lead compound: TGD001, investigated to provide a safe and effective treatment option for a broad range of thrombotic diseases. TargED aims to...

Medical Science Liaison - Oncology Pipeline (Netherlands) Company Overview A global biopharmaceutical company focused on advancing science, innovation, and technology to improve patient outcomes worldwide. The company develops and delivers specialty medicines, vaccines, and therapeutic solutions across multiple disease areas, including Oncology, Immunology,...

Territory Manager – Urology (Eastern & Central Netherlands) Location: Eastern & Central Netherlands, field-based, covering Utrecht, Nijmegen & Apeldoorn Employment type: Permanent, full-time (40 hours) Job Reference: 149 Package: [Salary + bonus + company car + benefits] About the company Our client is a leading global medical technology company with a...

Role Overview The position is for a Role Overview The position is for a Director, EU/ROW Regulatory Lead within the Global Regulatory Affairs team. The role involves representing Regulatory Affairs (RA) in Clinical Trial Teams, overseeing clinical trial submission activities, and working closely with CROs and internal stakeholders to ensure regulatory...

PSI is a leading Contract Research Organization (CRO) with about 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake...