clinical trial assistant

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....

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)...

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...

BeOne seeks a Regional Clinical Compliance Country Manager to oversee country- and site-level GCP compliance. You will apply risk-based methods to identify and manage compliance risks and partner with regional and global teams to safeguard patient safety and data integrity.The role includes leading site risk assessments, supporting CAPAs, and contributing to...

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...

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...

IQVIA LLC is seeking a Clinical Project Manager to lead delivery of local clinical studies, ensuring timelines, quality and cost targets are met. The role requires close collaboration with cross-functional teams and ongoing client coordination.The ideal candidate will have 5+ years of clinical research experience and strong knowledge of ICH GCP, with fluency...

IQVIA is seeking a Clinical Project Manager to deliver and manage smaller local studies with a focus on speed, quality, and cost efficiency. You will collaborate with clinical teams and cross-functional groups to ensure study milestones are met and customer expectations are fulfilled.The role requires strong communication in Dutch and English, adherence to...

uniQure in Amsterdam seeks a Director of Clinical Operations to drive end-to-end program success, aligning with the Head of Clinical Operations to ensure top quality, timelines and budgets. The role requires strong leadership across cross-functional teams and experience with international trial management.Responsibilities include feasibility, enrollment...

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...

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...

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...

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...

ProQR Therapeutics is seeking a Clinical Operations Lead in Leiden to drive end-to-end management of outsourced clinical trials, ensuring timelines, budgets, quality and regulatory compliance. You will safeguard data integrity and oversee the Trial Master File while coordinating with external vendors.The role requires 5+ years in clinical operations, strong...