Senior Clinical Data Manager – Trials

Company DescriptionPSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full-service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we...

Job Description Clincial Data Manager plays a critical role in the clinical research project. If you are detail-oriented and committed to quality, able to work with large volume of clinical or medical data, you might be the professional we are looking for.

PSI is a leading Contract Research Organization (CRO) with 30 years of experience in the pharmaceutical industry. Originated in Switzerland, PSI is a privately owned, full‐service CRO with a global reach, supporting clinical trials across multiple countries and continents. Our reputation for being highly selective about the projects we undertake highlights...

ICON plc is a world-leading healthcare intelligence and clinical research organization based in Milano.Possiede le competenze per ricoprire questo ruolo? Legga i dettagli completi qui sotto e invii la sua candidatura oggi stesso.We seek a Senior Global Project Manager to lead and deliver strategic trials, guiding cross-functional teams and stakeholders with...

The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client’s project team in the execution of clinical trials. Joining the team provides the opportunity to manage clinical research projects in different therapeutic areas and to cooperate closely with one of our key clients.We currently offer the...

ICON plc, a global healthcare intelligence and clinical research organisation, is seeking a Senior Clinical Research Associate to oversee monitoring of multicenter trials in Italy, ensuring protocol compliance and data integrity across sites. You will travel approximately 60% to sites, train staff, and resolve issues to drive quality and timely trial...

Job PurposeThe Clinical Trial Liaison Manager (CTLM) is responsible for site performance, trial delivery and Sponsor oversight across assigned countries. The CTLM ensures timely, high‑quality clinical trial execution, with a strong focus on patient recruitment, protocol adherence, regulatory compliance, and data quality.Acting as the primary Sponsor...

Overview As Project Manager at Alira Health, you will drive the efficient execution of study protocols within scope, budget, and regulatory guidelines. You will partner with the Clinical team, sponsors, and vendors to keep trials on track and deliver timely status updates. You’ll lead cross-functional study activities, oversee TMF processes, and support...

ICON plc, a global healthcare intelligence and clinical research organisation, is seeking a Senior Clinical Research Associate to oversee monitoring of multicenter trials in Italy, ensuring protocol compliance and data integrity across sites.You will travel approximately 60% to sites, train staff, and resolve issues to drive quality and timely trial...