Senior Pharmacology Scientist – Anti-Infectives

Qpex Biopharma, Inc

San Diego (CA)

Vor Ort

USD 140.000 - 170.000

Vollzeit

14 Tage+

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Zusammenfassung

Shionogi Inc. seeks a Scientist IV in Pharmacology to lead preclinical pharmacology studies across in vitro, ex vivo, and in vivo platforms.

You will interpret PK/PD and biomarker data to support antibacterial and antifungal programs through discovery and preclinical development. You will collaborate with microbiology, medicinal chemistry, and clinical development teams to ensure high-quality data, robust study designs, and regulatory-aligned documentation.

Qualifikationen

  • Ph.D. in microbiology, pharmacology, infectious disease biology, pharmaceutical sciences, biomedical sciences, or related with 5+ years of industry experience; or M.S. with 8+ years; or B.S. with 10+ years of experience.
  • Strong background in preclinical pharmacology, preferably antibacterial/antifungal/mycobacterial
  • Experience designing and interpreting in vitro and in vivo pharmacology studies including PK/PD

Aufgaben

  • Design, develop, and execute in vitro, ex vivo, and in vivo pharmacology studies to evaluate PK, efficacy, safety, and PD
  • Analyze and interpret pharmacology, PK, toxicology, efficacy, PK/PD, and biomarker data for dose rationale
  • Prepare study protocols, technical reports, and regulatory documentation
  • Collaborate with internal teams and CROs to coordinate study execution
  • Mentor junior scientists and review literature to improve study design

Kenntnisse

Data analysis
Scientific writing
Presentation
Communication

Ausbildung

Ph.D. in microbiology or related
M.S. in microbiology or related
B.S. in related field

Tools

PK/PD modeling software

Jobbeschreibung

Shionogi Inc. seeks a Scientist IV in Pharmacology to lead preclinical pharmacology studies across in vitro, ex vivo, and in vivo platforms.

You will interpret PK/PD and biomarker data to support antibacterial and antifungal programs through discovery and preclinical development. You will collaborate with microbiology, medicinal chemistry, and clinical development teams to ensure high-quality data, robust study designs, and regulatory-aligned documentation.

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