Principal Medical Writer
... Medical Point of contact for clinical regulatory stragegy As required, serves ... international regulatory submissions required like Clinical study reports, IBs, Protocols Experience ...
... Medical Point of contact for clinical regulatory stragegy As required, serves ... international regulatory submissions required like Clinical study reports, IBs, Protocols Experience ...
... methodology applicable in a non-clinical setting. Development and application of ... and QC. Liaise with internal Clinical Teams, external global Statisticians, vendors ... with application in a non-clinical setting. Strong understanding and knowledge ...
... to shape the future of clinical development. At ICON, it’s our ... . We want to be the Clinical Research Organisation that delivers excellence ... environment. • In depth experience within Clinical Research with experience in a ...
... to shape the future of clinical development. We are currently seeking ... role in designing and analyzing clinical trials, interpreting complex medical data, ... Core Docs and labeling for clinical trials. Collaborating with Regulatory Submissions ...
... to shape the future of clinical development. Senior or Principal Biostatistician ... role in designing and analyzing clinical trials, interpreting complex medical data, ... the statistical processes for multiple clinical studies. Effective written and oral ...
... communicate and negotiate timelines , including Clinical Budget Management and Regulatory Affairs ... expertise in managing high-volume clinical study start-up activities Strong ... governing the start-up of clinical trials B.S. or Advanced ...
... world-leading healthcare intelligence and clinical research organization. We’re proud to ... to shape the future of clinical development. At ICON, it’s our ... . We want to be the Clinical Research Organisation that delivers excellence ...
... world’s largest & most comprehensive clinical research organisation, powered by healthcare ... area contributors (e.g., Clinical, Pharmacovigilance, CPPM, etc.) and other ... experience and experience with clinical development regulatory documents preferred, with ...
... knowledge of Microsoft Office applications, Clinical Trial Management Systems, IVRS IWRS ... -5 years of experience supporting clinical trials. No In-House or ... skill in utilization of applicable clinical systems Experience in monitoring all ...
... to shape the future of clinical development. We are currently seeking ... a pivotal role in supporting clinical trial activities and collaborating with ... advantageous. Previous experience in a clinical research setting is preferred. Strong ...