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You will be responsible for providing, scientific leadership, and collaborative working environment to advance the drug candidates from IND through Phase IV. In addition, this position will collaborate with cross-functional stakeholders including in vitro & In vivo pharmacology, clinical biomarkers, DMPK, clinical development and operations, regulatory, CMC, and medical affairs.
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Ph. D. in Immunology, Hematology, Cancer Biology, Pharmacology, or related field. Expertise in the following techniques is mandatory: magnetic cell isolation, cell culture, phenotyping of bone marrow progenitors using multicolor flow cytometry, CFU assays using CD34+ cells, ELISA, MSD, Western blot for signaling pathway proteins, basic molecular biology including isolation of nucleic acid and real-time PCR.
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Practical knowledge and understanding of industry nomenclature; medical and procedural terminology; anatomy and physiology; pharmacology; and disease processes. Coding Certifications: The following are recognized professional certifications: Certified Professional Coder (CPC); Certified Outpatient Coder (COC); Certified Inpatient Coder (CIC); Certified Coding Specialist (CCS); or Certified Coding Specialist – Physician (CCS-P.
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Stay current with scientific advancements and regulatory trends in clinical pharmacology and Pharmacometrics, and apply the knowledge to advance drug discovery and development for the organization.
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