The qualified candidate must have at least a Doctor of Medicine or foreign equivalent degree in a medical, biological, pharmaceutical science or closely related field. The qualified candidate must have at least 2 years 24 months of experience working in a clinical setting with oncologyhematology drug development. The qualified candidate must have at least 2 years 24 months of experience with all the following a Contributing to the development of the program strategy for assigned trialscompounds; b Participating in the development of the clinical development plan CDP; c Leading clinical science activities from study startup through database lock leading into CSR writing and submission; d Reviewing ongoing summary hematologyoncology data including safety, primary efficacy variables, and laboratory data; e Directing the planning and implementation of clinical programs to meet corporate and clinicalbr research goals; f Facilitating CRO and site protocol trainings; and g Leading the response to protocol comments. All experience may be gained concurrently.

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