Responsibilities Performing site evaluation, initiation, monitoring and close-out visits, plus maintaining appropriate documentation according to a project-specific monitoring plan, ICH-GCP, and applicable regulations. Supporting the development of a subject recruitment plan. Establishing regular lines of communication
Clinical Research Associate (CRA) Job Description The Clinical Research Associate (CRA) is responsible for managing and monitoring the conduct of clinical projects according to ICH-GCP, Standard Operating Procedures (SOP), and applicable Project Management Plan (PMP) and local regulatory
Are you passionate about shaping the future of energy research and helping groundbreaking discoveries reach the global scientific community? Do you thrive on engaging with leading researchers, identifying emerging scientific trends, and influencing the direction of
Are you passionate about shaping the future of energy research and helping groundbreaking discoveries reach the global scientific community? Do you thrive on engaging with leading researchers, identifying emerging scientific trends, and influencing the direction of
Do you want to start a career as a scientific editor? Do you enjoy building trusted stakeholder relationships? About our Team Elsevier and the communities we support expand the possibilities of human progress. We champion scientific
Do you want to start a career as a scientific editor? Do you enjoy building trusted stakeholder relationships? About our Team Elsevier and the communities we support expand the possibilities of human progress. We champion scientific