Clinical Research Nurse: Lead Patient-Centric Trials

Premier Research is looking for a Senior Clinical Research Associate / Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly...

As Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites. This role focuses on delivering trials on time, in scope, and to high quality, within a global CRO environment. Your work...

Premier Research is looking for a Senior Clinical Research Associate / Clinical Research Associate II to join our Clinical Monitoring, Site Management and SSU team. You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly...

Clinical Research Coordinator in Milano Working Hours: 10 hours per week Start Date : ImmediatelyDuration : Approximately 6 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Rome. This 10h hour per week role offers a unique opportunity to contribute to meaningful research in a...

Overview Se i requisiti e l'esperienza richiesti per questo lavoro corrispondono alle sue competenze, la preghiamo di candidarsi tempestivamente. As Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs,...

Overview In this CRA role at Medpace you will support the integrity of clinical studies across pharmaceutical and medical device development. You’ll join a training-focused program (PACE) that accelerates your skills toward independent CRA responsibilities. You work across sites, regulators, and cross-functional teams to ensure compliant trials and data...

At 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 patients worldwide. As a...

Trial Form Support is seeking a Clinical Research Manager (CRM) in Ophthalmology to lead clinical operations across studies and countries within a global CRO environment. You will ensure ICH-GCP compliance, SOP adherence, and contracts while partnering with PMs, CRAs, sponsors, and sites.This home-based role offers exposure to cross-functional, international...

Overview In this role you will lead clinical trial monitoring to ensure protocol adherence, regulatory compliance, and high-quality data. You will work with cross-functional teams to enable timely trial execution and provide training to site staff. You’ll build strong relationships with site personnel to support smooth operations and continuous...