Senior CRA: Multi-Sponsor Clinical Trials

EPM Scientific, partnered with a leading Medical Device organisation in Europe, is seeking a Clinical Research Associate to oversee clinical study sites and ensure high-quality data collection. You will monitor sites, ensure regulatory compliance, and support patient recruitment while traveling up to 80% across assigned sites.Start date Jan 2027; 12-month...

Thermo Fisher Scientific is seeking a Principal Scientist in Biostatistics to advance life-changing therapies through statistical excellence.You will work within our Functional Service Provider division, applying advanced statistics across Phase I–III trials while collaborating with clients and regulatory authorities to ensure rigorous, compliant analyses...

The person providing these services is involved in clinical out of pocket (OOP) planning from the concept phase through execution and closeout and is responsible for clinical out of pocket cost forecasting and supporting budget creation and management for assigned projects.Essential FunctionsConduct monthly review and analysis of assigned projects, including...

IQVIA in Brussels, Belgium is seeking a Contract Negotiator 2 to develop investigator grants, contract language, and budgeting templates in support of proposal development and site contracting for clinical trials.You will coordinate with sponsors and study teams, ensure compliance with regulatory requirements, and mentor colleagues while maintaining...

CTI Clinical Trial and Consulting Services is seeking an experienced Clinical Research Associate to oversee monitoring activities at assigned study sites. The role includes site visits, regulatory document handling, and collaboration with sponsors and project teams to ensure quality and timelines.You will contribute to study start-up, patient enrollment...

Freelance Senior Clinical Research AssociateFull-timePSI 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.As a Senior CRA, you will work on the...

JoinExcelya,whereAudacity,Care,andEnergydefinewhoweareandhowwework.Webelieveincreatingboldsolutionsandfosteringaninclusiveenvironmentwherecollaborationandindividualgrowthgohandinhand. This

Serve as main CTI contact for assigned study sitesConduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in Monitoring Plan while adhering to all applicable regulatory requirements, SOPs and ICH GCPAssist with or oversee study...

For our client, a global medical device company, we are looking for a Clinical Research Associate. Position Summary The Clinical Research Associate (CRA) is responsible for monitoring and overseeing clinical investigations involving medical devices to ensure compliance with applicable regulations, Good Clinical Practice (GCP), study protocols, and company...