Global Clinical Study Lead

Astra Zeneca seeks a Senior Statistical Programmer II to lead the programming deliveries for clinical studies, ensuring quality and timely outputs. The role requires strong R and Python skills and the ability to guide cross-functional teams while adhering to industry standards. You will collaborate with statisticians, data managers and study leaders,...

Clinical Study Manager Maximice sus posibilidades de que su candidatura sea seleccionada asegurándose de que su CV y sus habilidades se ajustan al perfil. Spain, UK, Romania, Bulgaria, Czech Republic remoteAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As a Clinical Study Manager at ICON...

Clinical Study Manager - Sponsor Dedicated - Spain, UK, Romania, Bulgaria, Czech Republic - remoteAt 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...

Clinical Study Manager Maximice sus posibilidades de que su candidatura sea seleccionada asegurándose de que su CV y sus habilidades se ajustan al perfil. Spain, UK, Romania, Bulgaria, Czech Republic remoteAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As a Clinical Study Manager at ICON...

Clinical Study Manager Maximice sus posibilidades de que su candidatura sea seleccionada asegurándose de que su CV y sus habilidades se ajustan al perfil. Spain, UK, Romania, Bulgaria, Czech Republic remoteAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON's global expertise. As a Clinical Study Manager at ICON...

The Global Study Manager is a member of the extended global study team supporting delivery of clinical studies within BioPharmaceuticals Clincal Operations, Study Management to time, cost andquality, from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of Clinical Study Report (CSR) to study archiving. ...

Wodker Associates in Barcelona, Spain, seeks a CTP Manager to oversee disclosure of clinical trial information across registries and public websites, ensuring compliance with internal rules and external guidelines. You will develop and update the disclosure strategy, perform QA checks, and coordinate data collection and posting on company sites, with...

The Global Study Associate Manager (GSAM) is a role within Development Operations and is a member of the global study team supporting the delivery of clinical studies from Clinical Study Protocol (CSP) development through study set-up, maintenance, close-out, development of the Clinical Study Report (CSR), and study archiving. The GSAM works with internal...

The Global Study Associate (GSA) is a member of the extended Global Study Team, supporting the delivery of clinical studies within Late Development Oncology (LDO) to time, cost, and quality standards. The GSA supports clinical studies throughout their lifecycle, from Clinical Study Protocol (CSP) development and study set-up through maintenance, close-out,...