... limited to, clinical study design and protocol preparation, additional study or investigator documentation, contributions to data analysis plans, ongoing data interpretation, study reporting, and clinical development ...

... Responsible on certain projects. These activities include, but are not limited to, clinical study design and protocol preparation, additional study or investigator documentation, contributions to data analysis plans ...

... management of oncology phase 1 collaborators, consultants, and/or Clinical Research Organizations (CROs) in ... studying hematologic and solid tumor malignancies as well as for clinical research scientists leading all ...

... programs worldwide across all phases of clinical research. The Director will oversee study teams and will ... to be able to function independently in the daily management of clinical research projects including ...