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, on-site medical cover for high risk studies, and assessment of, reporting and acute management of potential adverse events Attend meetings related to the development and conduct of EM studies as agreed with
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and maintain appropriate academic, professional and industry contacts, including serving on Trial Steering Committees and Data Monitoring and Ethics Committees. Keep abreast of professional developments
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needed. The role will include responsibilities ranging from design, delivery and execution of the clinical trial, ensuring the safe conduct and collection of clinical data. The post provides an ideal
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-world data (RWD). This includes producing evidence to inform NICE’s Early Value Assessment (EVA) processes for HTE8 (depression) and HTE9 (anxiety) . Secondly, the Eli Lilly funded “Advancing
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throughout own work area. Desirable Interview / Application / Test Further Information Grade Grade 8 Salary £48,149-£57,422 with the potential to progress to £64,605 through sustained exceptional contribution