... Marketing for Medical Affairs trials. Actively contributes to process improvement; training and mentoring of Clinical Trial Administrators, Site Managers and other ... years of pharmaceutical and or clinical trial management experience is preferred. Specific ...
... Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management ...
... Associate Clinical Trial Manager (aCTM) to join our Clinical Trial Management team. The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management ...
... opinion leaders and physicians, overseeing Clinical Affairs investments and initiatives. Direct clinical trials across various regions, ensuring compliance ...
... and bid defense meetings Lead clinical resources in a matrix environment, as required, including Clinical Trial Assistants and Clinical Research Associates Set expectations for ...
... Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis ... provide medical oversight to the clinical trial program within your respective project ...
... Plan, Pediatric Investigational Plan, core Clinical Trial Protocols, input to Project Analysis ... provide medical oversight to the clinical trial program within your respective project ...
... ; Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred; 5+ years of Project Manager Clinical Trial Manager experience at a CRO ...
... sites to support the client’s clinical development programs Collaborate with internal ... to work on the client clinical trials Attend key therapeutic trainings meetings ... and related activities in a clinical trial Ability to have scientific discussions ...
... and ensuring consistent interpretation. Oversee clinical trials and Expanded Access Programs to ... and adverse event reporting within clinical trial settings. Solid knowledge of clinical trial design, regulatory standards, and drug ...