Through coordination with the Contract & Budget team, and collaboration with divisional and regional clinical teams, the CRA conducts clinical trial site start......To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of......Monitor on-site and remotely clinical trials in accordance with TFS and/or client company. Set up ISF and SMF (or cooperate with CTA) and distribute to the......Responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study initiation visits, regular visits and close out visits, assists......Anchored in our company's scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is......Our global Clinical Operations colleagues within our PPD clinical research services provide end-to-end support for clinical trials from study start up to......Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.E., Good Clinical Practice (GCP) and International......Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.E., Good Clinical Practice and International Conference on......The CTA is responsible for organizing and maintaining the Study Master File (SMF) and coordinating practical tasks during the study according to company......The Associate supports client engagements and internal project team requests and policy projects by developing research plans; conducting research; collecting......Validates study designs, is accountable for, and makes the final decision on the clinical/medical trial and program feasibility of implementing a clinical trial......Strong planning and organizational skills and the ability to work effectively and efficiently in a dynamic environment with competing projects and deadlines....COM is the department that manages clinical trials at the country level: identification and selection of sites, submission of dossiers for approval, start-up......AstraZeneca is an innovation-driven global biopharmaceutical company focused on the discovery, development and commercialization of prescription medicines,......By assisting in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST)......Support and act as the point of reference for Analysts in their daily activities and training, among others. Associate Consultants are involved in the execution......The Clinical Study Excellence Scientist (CSES) is the point of contact and responsibility for all aspects of a trial within the study team, with the aim of......
