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MEDICAL DIRECTOR OF NEUROSCIENCE

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Company: Bristol-Myers Squibb (bms)

Location: Princeton, NJ

Date Posted: July 22, 2014

Source: TAOnline

Designs and executes Phase I and II clinical trials of assets within the Genetically Defined Diseases (GDD) Therapeutic Area that target Neurodegenerative Diseases and Neuropathic Pain. These studies include those for target engagement and proof of mechanism/concept. Manages a matrix team including PhDs, Pharmacokineticists, and Clinical Scientists in the planning, execution, and interpretation of clinical trials and research and the data collection activities. Assists in the interpretation of clinical pharmacology profiling of drug candidates, including drug/drug interaction, age and gender, renal and hepatic impairment, food effect, and ADME Absorption Distribution Metabolic Excretion studies on healthy volunteers. Provide medical expertise on compounds in development and in life cycle management. Strategic contribution to the whole therapeutic area (TA) from discovery to early clinical development up to Phase
2. Serve as one of the company's scientific and medical experts for the relevant area of medical expertise. Represent to the highest ...
Designs and executes Phase I and II clinical trials of assets within the Genetically Defined Diseases (GDD) Therapeutic Area that target Neurodegenerative Diseases and Neuropathic Pain. These studies include those for target engagement and proof of mechanism/concept. Manages a matrix team including PhDs, Pharmacokineticists, and Clinical Scientists in the planning, execution, and interpretation of clinical trials and research and the data collection activities. Assists in the interpretation of clinical pharmacology profiling of drug candidates, including drug/drug interaction, age and gender, renal and hepatic impairment, food effect, and ADME Absorption Distribution Metabolic Excretion studies on healthy volunteers. Provide medical expertise on compounds in development and in life cycle management. Strategic contribution to the whole therapeutic area (TA) from discovery to early clinical development up to Phase
2. Serve as one of the company's scientific and medical experts for the relevant area of medical expertise. Represent to the highest standard BMS at public forums, advisory boards as well authoring scientific publication in leading medical journals. Contributes to the writing, review and publishing of reports submitted to regulatory agencies. Identify and build relationships with thought leaders and principal investigators and gather input on disease areas and design of clinical programs. Participates in licensing teams in the evaluation of clinical or preclinical external opportunities. Contributes to continuous improvement initiatives, effective team-building and effective communication across the BMS community. , ,
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