... :The Clinical Trial Supply (CTS) Senior Study Manager is responsible for managing the end-to-end supply chain for assigned clinical studies throughout the multi-year study lifecycle. The CTS Senior Study Manager independently leads clinical studies ...
... our inhouse and remote Lead Clinical Research Associates Clinical Research Associates and Clinical Trial Associates.The Manager Clinical Field Operations EMEA is expected ...
... our inhouse and remote Lead Clinical Research Associates Clinical Research Associates and Clinical Trial Associates. The Manager Clinical Field Operations EMEA is expected ...
... into the Head of Global Supply Chain & External Supply Integration and 7 Managers will report into you.The RoleProvide strategic leadership and deliver of an efficient, cost-effective clinical trial supply chain for CSLs clinical programs.You will be ...
... interact with QA, Global Monitoring, clinical Study Start-Up teams, Global Clinical Trial Managers (CTMs), Global Regulatory and other ...
... logistical support to the Project Manager of clinical trials to coordinate all study-related activitiesAssists with other project specific tasks as delegated by Project Manager.May assist as back-up for Project Manager when feasible, being the primary ...
... of the EMEA-Clinical Project Managers (CPMs) and other direct reports related to the design, management, and execution of clinical studies for worldwide product approval ... management to ensure that clinical trial-related tasks, milestones, and deliverables ...
... Management (permanent, fulltime). The Program Manager, Clinical Supply Chain Management’s primary responsibility is to manage the clinical supply chain for early phase (uncomplicated) compounds. The completion of clinical trials is the rate-limiting step ...
... Management (permanent, fulltime). The Program Manager, Clinical Supply Chain Management’s primary responsibility is to manage the clinical supply chain for early phase (uncomplicated) compounds. The completion of clinical trials is the rate-limiting step ...
... examine ways to enhance overall clinical trial performance.Facilitate communication between clinical sites and other Abbott clinical staff (e.g., CSL, CRA, ... : technical, protocol, standard of care, clinical trial reimbursement, etc.Responsible for product ...