Intern Clinical Study Management
... work in the arena of Clinical Trial ManagementbrThe Student will: br * Learn and support clinical trial management needs on specific clinical trials, working with the assigned project ...
... work in the arena of Clinical Trial ManagementbrThe Student will: br * Learn and support clinical trial management needs on specific clinical trials, working with the assigned project ...
... ) Director, this job within Global Clinical Delivery (GCD) combines end-to-end design, execution, and reporting of clinical trials with leadership in project teams ... global study teams in Oncology clinical trials.br * Proactively identify and resolve ...
... strategic operational insights to clinical trial teams, leveraging their capabilities in ... business reviews and early clinical trial planning * Support the identification of appropriate sites and countries for trial placement * Acquire, aggregate and or ...
... and available to respond to monitors during all types of monitoring ... -the-job experience in a clinical trial environment, where relevant experience has been gained in clinical trials, clinical terminology, and medical research working ...
... subject matter knowledge as you monitor the progress of clinical trials at the site level and ... to perform studies and initiate clinical trials.br * Ensures recruitment and retention ...
... , execution, and delivery of the Clinical trial in the country.In this ... ensure best possible outcome for Clinical Trial Applications (CTAs) following EU CTR. * ... understanding of global and local clinical trials regulations and start-up processes * ...
... relationships with partners to drive clinical pharmacology excellencebrbrWHO YOU AREbrbr* PhD, ... expertise in the area of Clinical Pharmacology and Oncology Drug Development; ... of development projects from a Clinical Pharmacology perspective brbr* Evidence of ...
... * Knowledge of a scientific or clinical areabr * Knowledge of clinical trial design and processbr * Knowledge of ... inclusive culture, promoting diversity in clinical trials, while our shared values of ...
... for filing in the Trial Master File (TMF) and verify that the Investigators Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) International Conference on ... of degree.br * Prior clinical experience preferred.br * Computer skills ...
... requiredbr * Manages and tracks:br * clinical non-clinical suppliesbr * patient recruitmentbr * study metricsbr * Coordinates and manages meetings with investigator sites, site monitors, including preparing meeting materials and ...