Senior Clinical Trial Associate

Job DescriptionThe Sr CRA is an important member of the Alira Health Clinical team. The Sr CRA is highly motivated and functions independently to conduct site monitoring responsibilities for clinical trials to ensure compliance and quality. The Sr CRA works closely with US: Director of Clinical Monitoring, Lead CRAs, in-house CRAs, EU: Associate Director of

Alira Health SAS is seeking a Senior Clinical Research Associate to lead monitoring activities across clinical trials. You will collaborate with regional directors, Lead CRAs, and project managers to ensure protocol compliance, site questions, and timely study execution.The role requires strong organizational and leadership skills, willingness to travel, and...

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development. As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they

ICON plc is a world-leading healthcare intelligence and clinical research organization seeking a Senior CRA to oversee clinical trial activities to ensure compliance with protocol, regulatory requirements, and industry standards.You will lead monitoring tasks focusing on quality and continuous improvement, perform site visits, collaborate across functions,...

Who We AreWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.Who We

Worldwide Clinical Trials is seeking a Senior Clinical Research Associate (CTM/CR A) to lead local and regional site management teams across oncology studies. The role includes mentoring CRA staff, coordinating with sponsors and investigators, and ensuring quality and compliance through monitoring plans and visits.Travel is required to support sites and...

Due to growth, we have an immediate need for an experienced freelance (up to 1 FTE) CRA, French speaking, to join our growing global team, based in France. Main Responsibilities: Responsible for conduct of all types of monitoring, and co-monitoring visits and associated monitoring activities for assigned

Who we areWe're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global

ProPharma Group is seeking an experienced Clinical Research Associate (freelance, up to 1 FTE) to join our France-based team. The role covers on-site and remote monitoring, site initiation, and close-out visits, ensuring compliance with SOPs and local regulations.You will support start-up activities, prepare trackers, and collaborate with site staff,...