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Senior Scientist I, DMPK, to apply, click here,

Vir Biotechnology

    • Evaluate the PK properties of our drug candidates by selecting, designing and managing in vivo studies (in-house or outsourced) as well as overseeing and participating to the sample bioanalysis.
    • Analyze, summarize, interpret and present study results to project teams.
    • Ensure adherence to the highest quality standards and quick turnaround times.
    • Maintain up-to-date knowledge in advancements in DMPK, and apply to the development of new capabilities/strategies where appropriate.
    • Keep quality electronic records and upload data into company databases.
    • Build, manage and mentor a small team of Junior members.
    • Author reports and documents in support of regulatory filing efforts.
    • Be a key DMPK contributor in multidisciplinary team meetings by providing subject matter expertise to help advancing drug candidates through discovery and development.

    • PhD in a relevant field with 4+ years’ industry R&D experience, MS with a minimum of 8+ years of experience, or BS with a minimum of 10+ years preferred.
    • Demonstrated hands-on experience with small molecule quantitative bioanalysis by LC/MS, as well as PK data analysis and reporting
    • Familiarity with DMPK techniques, methodologies and workflows; clear understanding of ADME/PK principles and strategies in drug discovery and preclinical development.
    • Experience formally managing direct reports is required.
    • Knowledge and experience with discovery-level compound formulation a plus.
    • Experience with supporting regulatory activities.

Location: Saint Louis, MO


Post Date: 3/31/2022 12:00:00 AM
┬ęPharmaceutical & BioScience Society, International; Last Modified: 5/17/2022; Admin Logon
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