clinical trial manager

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...

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...

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...

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...

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;...

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...

Verbatim Pharma in Amsterdam is seeking a Clinical Supply Project Manager to lead multiple global clinical trial projects in a hybrid work setting. You will liaise with clients, coordinate timelines, and drive deliverables across cross-functional teams to ensure regulatory and quality standards are met.The role demands 2+ years in pharma or clinical...

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...

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)...

Medpace is seeking a full-time, office-based Associate Director to join our Commercial Operations team in Maastricht. You will work on a team to accomplish tasks and projects that are instrumental to the company’s success.If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the...

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)...

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...

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...

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...

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...

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...

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...