Kappaalphapsi1911
In Vivo Respiratory Principal Scientist
Kappaalphapsi1911, Collegeville, Pennsylvania, United States, 19426
Overview
As a lab-based In Vivo Respiratory Principal Scientist in the Complex Models group within the Respiratory, Immunology & Inflammation Biology Unit (RIIBU), you will contribute to the in vivo biology strategy and lead the design, execution, and reporting of preclinical integrative experiments to support therapeutic area teams and drug discovery projects from target validation through to clinical phases. You will have the opportunity to work on targets, in vivo models, and integrative, translational biology relevant to respiratory diseases such as COPD and IPF/ILD. Key Accountabilities / Responsibilities
Contribute to the design and lab/vivarium-based execution of in vivo strategies for the respiratory disease area. Contribute to the delivery of respiratory preclinical efficacy and mechanistic in vivo studies using respiratory models to enable PK/PD and translational biomarker data generation. Lead discussions to ascertain a robust understanding of scientific rationale, key objectives, endpoints and Go/No-Go decisions for in vivo models and studies, setting clear goals and timelines. Use understanding of PK/PD principles relating to respiratory diseases to drive innovation and independently design, execute, analyze, and present in vivo studies as the In Vivo Leader (IVL) representative on portfolio projects with input from Biology Leader (BL), Project Leader (PL), and Complex Models Leadership Team. Understand and independently apply robust study design (RSD) principles, gain input from Subject Matter Experts and matrix partners prior to seeking endorsement/recommendations for animal studies at Independent Scientific Review forum and Pre-Study Briefings. Anticipate potential challenges with experiments and independently resolve technical issues in planning, setup, and execution with minimal guidance. Lab/vivarium-based execution to enable sample/tissue acquisition, processing, and analysis to enable integration of PK/PD and translational biomarker data from in vivo studies and where necessary utilize advanced ex vivo assay techniques such as flow cytometry, ELISAs, MSD, Luminex and qPCR. Act as key contact for animal studies, including provision of out of hours procedures as required. Maintain technical expertise in animal handling, dosing, blood and tissue collection, and measurements of biological/physiological function (e.g., lung function, hemodynamics). Be familiar with federal laws surrounding animal use in research and the local governance process (IACUC, AUP). Be familiar with severity limits/constraints related to adverse effects and respond as required under IACUC, AUP and policy on care, welfare and treatment of animals. Assess animal health and welfare, document findings, and act on them or seek expert advice when necessary. Work effectively with internal matrix partners (e.g., BL, PL, RTech). Lead external animal studies (e.g., CRO, academic groups) including study monitoring responsibilities. Maintain accurate, up to date electronic laboratory records in alignment with data integrity standards and ensure compliance with SOPs, risk assessments and safety guidelines. Foster an enterprise culture of innovation, collaboration, inclusion, and continuous learning. Keep up to date with the relevant literature and apply to in vivo strategies and studies. Basic Qualifications, Knowledge, Skills, and Experience
BSc in a biological science with 5+ years of respiratory in vivo experience, or a Masters in Biological Science with 4+ years of respiratory in vivo experience, or a PhD in biological science with 2+ years of respiratory in vivo experience, in industry or academia. Current experience and knowledge of respiratory disease mechanisms involved in COPD and IPF/ILD and use of in vivo systems to interrogate pathophysiological mechanisms in these diseases. Hands-on experience with animal model systems in the respiratory disease area including lung function measurement (e.g., whole-body plethysmography, dynamic compliance and resistance, FEV and FVC). Experience in using in vivo models in the respiratory disease area including animal handling, dosing (intranasal and intra-tracheal), tissue necropsy (BAL and lung dissection), and blood sampling. Experience with flow cytometry (processing of respiratory-relevant tissues), ELISAs, MSD, Luminex and qPCR or RNAseq. Experience overseeing external animal studies conducted at CROs or academic groups as study monitor. Experience writing and critiquing scientific documents and independently communicating scientific ideas and experimental findings to line and matrix teams. Preferred Requirements
Expertise in biomarker assay development in the respiratory disease area to define PKPD parameters and inform translational research. Experience in drug discovery processes within the pharmaceutical or biotech industry and knowledge of the drug discovery pillars. Familiarity with omics platforms (spatial, bulk and single cell RNA seq) and advanced imaging technologies. Proven ability to balance multiple priorities and meet deadlines. Knowledge of regulatory guidelines relating to use of animals in research and compliance requirements. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, parental status, national origin, age, disability, genetic information, military service or any basis prohibited under federal, state or local law. Please note that if you are a US Licensed Healthcare Professional, GSK may be required to capture and report expenses in the event you are afforded an interview for employment. For more information, please visit the CMS Open Payments data website.
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As a lab-based In Vivo Respiratory Principal Scientist in the Complex Models group within the Respiratory, Immunology & Inflammation Biology Unit (RIIBU), you will contribute to the in vivo biology strategy and lead the design, execution, and reporting of preclinical integrative experiments to support therapeutic area teams and drug discovery projects from target validation through to clinical phases. You will have the opportunity to work on targets, in vivo models, and integrative, translational biology relevant to respiratory diseases such as COPD and IPF/ILD. Key Accountabilities / Responsibilities
Contribute to the design and lab/vivarium-based execution of in vivo strategies for the respiratory disease area. Contribute to the delivery of respiratory preclinical efficacy and mechanistic in vivo studies using respiratory models to enable PK/PD and translational biomarker data generation. Lead discussions to ascertain a robust understanding of scientific rationale, key objectives, endpoints and Go/No-Go decisions for in vivo models and studies, setting clear goals and timelines. Use understanding of PK/PD principles relating to respiratory diseases to drive innovation and independently design, execute, analyze, and present in vivo studies as the In Vivo Leader (IVL) representative on portfolio projects with input from Biology Leader (BL), Project Leader (PL), and Complex Models Leadership Team. Understand and independently apply robust study design (RSD) principles, gain input from Subject Matter Experts and matrix partners prior to seeking endorsement/recommendations for animal studies at Independent Scientific Review forum and Pre-Study Briefings. Anticipate potential challenges with experiments and independently resolve technical issues in planning, setup, and execution with minimal guidance. Lab/vivarium-based execution to enable sample/tissue acquisition, processing, and analysis to enable integration of PK/PD and translational biomarker data from in vivo studies and where necessary utilize advanced ex vivo assay techniques such as flow cytometry, ELISAs, MSD, Luminex and qPCR. Act as key contact for animal studies, including provision of out of hours procedures as required. Maintain technical expertise in animal handling, dosing, blood and tissue collection, and measurements of biological/physiological function (e.g., lung function, hemodynamics). Be familiar with federal laws surrounding animal use in research and the local governance process (IACUC, AUP). Be familiar with severity limits/constraints related to adverse effects and respond as required under IACUC, AUP and policy on care, welfare and treatment of animals. Assess animal health and welfare, document findings, and act on them or seek expert advice when necessary. Work effectively with internal matrix partners (e.g., BL, PL, RTech). Lead external animal studies (e.g., CRO, academic groups) including study monitoring responsibilities. Maintain accurate, up to date electronic laboratory records in alignment with data integrity standards and ensure compliance with SOPs, risk assessments and safety guidelines. Foster an enterprise culture of innovation, collaboration, inclusion, and continuous learning. Keep up to date with the relevant literature and apply to in vivo strategies and studies. Basic Qualifications, Knowledge, Skills, and Experience
BSc in a biological science with 5+ years of respiratory in vivo experience, or a Masters in Biological Science with 4+ years of respiratory in vivo experience, or a PhD in biological science with 2+ years of respiratory in vivo experience, in industry or academia. Current experience and knowledge of respiratory disease mechanisms involved in COPD and IPF/ILD and use of in vivo systems to interrogate pathophysiological mechanisms in these diseases. Hands-on experience with animal model systems in the respiratory disease area including lung function measurement (e.g., whole-body plethysmography, dynamic compliance and resistance, FEV and FVC). Experience in using in vivo models in the respiratory disease area including animal handling, dosing (intranasal and intra-tracheal), tissue necropsy (BAL and lung dissection), and blood sampling. Experience with flow cytometry (processing of respiratory-relevant tissues), ELISAs, MSD, Luminex and qPCR or RNAseq. Experience overseeing external animal studies conducted at CROs or academic groups as study monitor. Experience writing and critiquing scientific documents and independently communicating scientific ideas and experimental findings to line and matrix teams. Preferred Requirements
Expertise in biomarker assay development in the respiratory disease area to define PKPD parameters and inform translational research. Experience in drug discovery processes within the pharmaceutical or biotech industry and knowledge of the drug discovery pillars. Familiarity with omics platforms (spatial, bulk and single cell RNA seq) and advanced imaging technologies. Proven ability to balance multiple priorities and meet deadlines. Knowledge of regulatory guidelines relating to use of animals in research and compliance requirements. GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, gender identity, sexual orientation, parental status, national origin, age, disability, genetic information, military service or any basis prohibited under federal, state or local law. Please note that if you are a US Licensed Healthcare Professional, GSK may be required to capture and report expenses in the event you are afforded an interview for employment. For more information, please visit the CMS Open Payments data website.
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