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    Principal Scientist/Associate Director of Pharmacology

    • Juvena Therapeutics
    • Full time
    • Redwood City, California
    • Posted: January 11, 2023
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    Company
    Juvena Therapeutics

    Position Description

    Juvena Therapeutics is seeking a talented scientific strategist and experienced people leader to lead their pharmacology team as well as early preclinical validation of lead candidates. We are searching for an individual who is excited to work as a leader in an intimate and small team focused on the discovery, preclinical validation, and clinical translation of novel biologics for chronic and rare degenerative diseases across multiple therapeutic areas such as neuromuscular, inflammatory, hepatic, and metabolic-related diseases. This position would oversee the in vivo pharmacology efforts at Juvena with a particular focus on preclinical disease model development, design and implementation of in vivo studies. The Principal Scientist/ Associate Director of Pharmacology will work closely with the department heads across data sciences, discovery, nonclinical and clinical teams to expand Juvena’s platform and execute on critical in vivo studies for unraveling secretome biology to develop novel disease-modifying biologics. The Principal Scientist/ Associate Director of Pharmacology will work collaboratively with various functions to establish robust disease model systems to support ongoing projects and validation of protein pharmaceutical drug candidates. Reporting to the SVP of Discovery, the  Principal Scientist/ Associate Director of  Pharmacology will be involved in diverse drug candidates in Juvena’s pipeline as well as establishing external R&D partnerships with academic institutions and technology providers.

    *Title commensurate with experience.

    Company Summary

    Juvena Therapeutics is on a mission to discover and develop biologics for rare and chronic degenerative diseases by mining the secretomes of human pluripotent stem cells through a machine learning (ML)-enhanced platform. Juvena’s approach integrates proteomics, transcriptomics and imaging with phenotypic human in vitro disease model screening and extensive preclinical validation to mine stem cell secretomes as a rich source of new medicines for chronic and rare diseases. We are advancing leads for muscular dystrophies, muscle atrophy, injury, and osteopathies. Since our launch in mid-2018, Juvena has discovered 17 hits for neuromuscular and skeletal diseases, including several muscle regenerative protein therapeutic candidates with potent human in vitro and mice in vivo efficacy. Juvena is advancing a lead program for Myotonic Dystrophy Type 1, a rare autosomal dominant, progressive muscle-wasting disease.

    Juvena Therapeutics has secured venture capital, NIH, and CIRM funding to develop their top lead to a clinical-stage investigational new drug, to build their stem cell secretome database, and to leverage their discovery platform to rapidly identify and validate novel protein-based drug candidates for multiple rare and chronic diseases across inflammatory, cardiometabolic and hepatic therapeutic areas. At Juvena we embrace a diversity of backgrounds, experiences, and approaches that all combine to lead us to world-class scientific results in an inclusive environment.

    Major Responsibilities

    • Lead efforts to expand Juvena’s in vivo pharmacology capabilities across multiple organ model systems to support growth of our biologics platform
    • Work closely with the preclinical team members to design and execute in vivo experiments to support research and development of Juvena’s drug candidates for treatment of various rare and chronic degenerative diseases
    • Manage lab associates/scientists to deliver high-quality results in a fast-paced setting
    • Design and execute experiments following appropriate laboratory procedures and guidelines
    • Must be proficient in murine handling, dosing (PO, IV, IP, SC), survival and terminal blood collection (SM, tail nick, cardiac puncture), and tissue harvesting at necropsy including fixation, freezing and tissue disaggregation to support ex vivo analyses
    • Work closely with the nonclinical development team to establish translational capabilities for transition of lead drug candidates into the clinical development
    • Support IND-enabling studies for biologics, internally and externally via CRO project management across all phases of Juvena’s discovery and development
    • Perform tissue processing for molecular, biochemical and histological analysis
    • Carry out high throughput staining and image analysis
    • Prepare presentations, technical reports, summaries, protocols
    • Keep current with advances in the company’s area of research interest and lead journal club discussions of latest literature and research discoveries
    • Contribute to a dynamic and exciting culture that embraces teamwork and innovation

    Position Requirements and Experience

    • PhD with 6+ years of industry experience (or equivalent) in drug discovery and early development setting
    • Demonstrated ability to advance programs from discovery through lead identification and IND with biologics such as fusion proteins, bispecifics, antibody or antibody drug conjugates, preferably in the regenerative medicine space and/or inflammatory, cardiovascular, metabolic disease areas
    • Understanding of how in vivo pharmacology data fits into bioinformatics and machine learning applications for drug discovery, target identification and validation
    • Experience in GMP/GLP documentation and IND filing
    • Experience interfacing with multiple key stakeholders in a dynamic environment to enable real-time prioritization
    • Strong communication skills
    • Highly self-motivated, independent, and driven to succeed
    • Prior success with research in a hands-on, highly collaborative growth environment
    • The ability to work effectively both independently and as part of multidisciplinary team in a fast-paced environment

    Preferred Qualifications

    • Documented experience in regenerative medicine
    • Successful track record of indication selection and prioritization analyses
    • Direct experience in managing IND-enabling studies with significant contribution to FDA-approved INDs
    • Familiarity with pre-commercial process

    Compensation and Benefits

    • Competitive salary, annual bonus and stock options
    • Health/Dental/Vision insurance
    • Paid vacation and holidays
    • Partial 401K matching
    • Clinical Scientist
    • Clinical Development
    • Research Scientist

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