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Sr Scientist I: BS in molecular biology, biochemistry, pharmacology, or a related field with typically 10+ years of experience, MS and typically 8+ years of experience, or PhD and typically 0+ years of experience, preferably in the areas of cellular assay development and screening.
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The applicant is expected to develop highly effective collaborations with relevant stakeholders including those in Patient Health & Impact, the Patient-Centered Outcomes Assessment Group, Statistics, Clinical Pharmacology, Clinical Development, Medical Affairs, Epidemiology, Programming, and other groups contributing to HEOR analysis and strategy.
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Serve as a QTAS representative on project teams supporting the development of novel biologics; collaborate with project team members (e.g., clinical pharmacology, protein analytics, discovery, toxicology) and groups within QTAS to generate relevant data guiding target validation, biomarker selection, and candidate selection.
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Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance. MD / DO with 2+ years of residency with patient management experience; Master Public Health is preferred in addition to MD / DO, not required.
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Bachelors degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology) math, engineering, or medical fields is preferred. Bachelors degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology) math, engineering, or medical fields is preferred.
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Knowledge in anatomy and physiology, medical terminology, pathology and disease processes, pharmacology, health record format and content, reimbursement methodologies and conventions, rules and guidelines for current classification systems (ICD, CPT, HCPCS.
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Bachelor's Degree required in pharmacy, biology, chemistry, pharmacology, engineering or related subject. Bachelor's Degree required in pharmacy, biology, chemistry, pharmacology, engineering or related subject.
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