clinical trial

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...

Medpace, Inc. is seeking a full-time, office-based Account Manager for our Commercial Operations team in Maastricht. You will work with a team to drive bids, oversee financial and contractual performance, and maintain strong client relationships during clinical trials.The role requires a Bachelor's degree in Business, Finance, or Accounting and 5 years of...

Maastricht UMC+ zoekt een Legal Counsel Research die onderzoekers en CTCM-collega’s ondersteunt bij voorbereiding, contractering en uitvoering van mensgebonden wetenschappelijk onderzoek. Je beoordeelt contracten en adviseert over privacy, aansprakelijkheid, IP en naleving van gedragscodes.Je ontwikkelt standaard contracten, modelclausules en richtlijnen;...

The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions and is accountable for the statistical deliverables within the program.(There are 2 positions available supporting multiple Therapeutic Areas)...

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...

De functie Als Legal Counsel Research werk je binnen de afdeling Research Project Support. Je ondersteunt en adviseert onderzoekers van het Maastricht UMC+ en collega’s van CTCM bij de voorbereiding, contractering en uitvoering van mensgebonden wetenschappelijk onderzoek. Je stelt onderzoekscontracten op en beoordeelt deze en adviseert over juridische...

De functie Als Legal Counsel Research werk je binnen de afdeling Research Project Support. Je ondersteunt en adviseert onderzoekers van het Maastricht UMC+ en collega’s van CTCM bij de voorbereiding, contractering en uitvoering van mensgebonden wetenschappelijk onderzoek. Je stelt onderzoekscontracten op en beoordeelt deze en adviseert over juridische...

A global clinical research organization is seeking a Psychiatry Medical Director to lead medical, scientific, and strategic aspects of clinical trials. This role requires an M.D. degree, with board certification preferred. Responsibilities include providing medical management, contributing to study reports, and ensuring safety in trials. Hybrid work is an...

ICON Strategic Solutions is seeking a Feasibility Analytics Manager to lead analytics and enrollment modelling for global clinical trials in a sponsor-dedicated model based in Groningen, NL.You will collaborate with Global Feasibility leads and Data Sciences to deliver data-driven insights, implement new technologies, and ensure high-quality analytic...

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...

CHDR Twente zoekt een Director Twente die de vestiging verder uitbouwt en professionaliseert. Je draagt eindverantwoordelijkheid voor groei, onderhoudt verbindingen met Leiden en regionale partners en rapporteert rechtstreeks aan de CEO.Je combineert wetenschappelijke senioriteit met bedrijfsvoering: PhD en klinisch onderzoeksverleden, GCP-kennis, en...

Medpace, Inc. in London seeks a Hepatologist to provide medical leadership for clinical trials, review results, and guide study design and project plans. The Medical Monitor will serve as the medical expert for interpretation of trial results and contribute to regulatory documents.All Medical Monitors have hybrid WFH flexibility, with travel up to 20%. The...

Medpace, a global CRO, seeks a Dermatologist - Medical Director to provide leadership for planning, execution, and reporting of clinical trials. This role acts as an internal medical expert for review, presentation, and interpretation of results in the Clinical Study Report and participates in study design and project planning.All Medical Directors have...

Why Join Clinical Functional Service Partnerships (CFSP)? At IQVIA, our Clinical Functional Service Partnership (CFSP) model gives you the best of both worlds: the variety and sponsor-level exposure of working as an embedded member of a leading pharmaceutical or biotechnology team, backed by the stability, global infrastructure, and career support of IQVIA....

Centre for Human Drug Research (CHDR) in Leiden, the Netherlands, is seeking an experienced Software Engineer to help enhance Promasys, a core data platform for clinical trial management. You will design, build, and maintain backend services and Flutter-based applications that enable accurate and efficient clinical research, working closely with researchers...

Company DescriptionWe are the company that cares; for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who...

CHDR in Leiden zoekt (bijna) afgestudeerde arts-onderzoekers die klinisch geneesmiddelenonderzoek willen combineren met wetenschap en leiderschap. Je combineert artsenrol met projectleiding en werkt nauw samen met onderzoekers en (inter)nationaal farmaceutische opdrachtgevers.Je zet klinische studies op, coördineert uitvoering, analyseert data en denkt mee...

Praxa Sense is seeking a Lead Clinical Research to organize and guide the clinical and experimental validation of our optical sensing technology. You will design trials, coordinate approvals, and ensure high-quality data to validate our platform for health monitoring.You will work with hospitals, research institutes, and the R&D team to align clinical...

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...

ProQR Therapeutics in Leiden, NL is seeking a Clinical Operations Lead (full-time) to direct end-to-end management of outsourced clinical trials, ensuring data integrity and patient safety.You will serve as the operational lead for the trial team, liaising with CROs, managing timelines and budgets, and upholding ICH-GCP and EMA/FDA regulations.The role...