Senior Scientist, In Vitro Cardiometabolic Disease
Pharma
Job description
Job Description Our company's South San Francisco research laboratory is seeking a highly motivated, energetic, and skilled Senior Scientist (R3) with a strong in-vitro background in biology, biochemistry, or pharmacology to join the Cardio-Metabolic Disease (CMD) department. This is a hands-on, lab-facing role, providing in-vitro expertise to metabolic and endocrine disease-related exploratory and pipeline programs, with flexible skill sets to meet our current and future needs. The individual will independently design, execute, analyze, and interpret complex in-vitro studies to support target identification, validation, and therapeutic development. The successful candidate will also possess a strong sense of intellectual curiosity to expand their technical expertise at the bench, as well as effective written and interpersonal communication skills to explain complex experiments and biological concepts to a broader scientific team. Key Responsibilities: Design, perform, troubleshoot, document, analyze, and interpret in-vitro experiments, with minimal supervision, to support and/or lead multiple exploratory activities and pipeline projects. Develop and validate complex in-vitro models and establish sets of in-vitro assays, suitable for the mechanistic investigation of potential targets, as well as evaluation of therapeutic candidates, for metabolic and endocrine diseases. Work independently in executing tightly controlled experiments and presenting high-quality data to multi-disciplinary project teams. Identify and implement opportunities to reduce timelines, improve throughput, and increase operational efficiency. Stay current with emerging scientific and technological advances relevant to metabolic and endocrine diseases. Contribute to the internal and external scientific visibility of the Obesity and Metabolism Group through presentations, publications, and scientific engagement. QUALIFICATIONS: Education: Bachelor’s (with 7+ years), or Master’s (with 4+ years) in Biology, Biochemistry, Pharmacology, or related discipline with the indicated years of relevant industry experience. Required Experience and Skills: Experience in more than one of the following areas: target identification, target validation, quantitative assay development, metabolic diseases, neuro-endocrine diseases. Expertise in working with more than one type of disease-relevant human primary cell or cell line (e.g. adipocytes, hepatocytes, myocytes, osteocytes, endocrine cells) in both routine and complex assay systems. Demonstrated ability to manage multiple projects and competing priorities while maintaining scientific rigor and attention to detail. Professional level of communication of data, with skills in collaboration and cross-functional partnership. Deep scientific curiosity and analytical mindset with a drive to understand biology and mechanism of action, while aligning their work with project goals and business needs. Preferred Experience and Skills: Experience working with GPCR targets, and developing quantitative, 96-well and 384-well plate cell-based assays. Mastered several standard biochemistry and molecular biology techniques (e.g. mRNA isolation, qRT-PCR, ELISA, HTRF, AphaLISA, Our company, western-blotting). Expertise in developing metabolic disease-relevant in-vitro phenotypic and functional assays (e.g. calcium flux, cAMP/IP1 accumulation, beta-arrestin, receptor dimerization, glucose uptake, lipid uptake, lipolysis, Seahorse, high-content imaging through cell-painting or immunofluorescence staining). Vast experience in titrating various modes of target modulation (e.g. small molecules, peptides, antibodies, antibody-peptide conjugates, siRNA, viral-vectors). Demonstrated ability to employ AI agents and LLMs for hypothesis generation, literature synthesis, experimental design, complex data analysis, or competitive intelligence. #EligibleforERP Required Skills: Assay Development, Biochemical Assays, Cell Culture Techniques, Drug Target Identification, High Content Screening, Immunoassays, Immunology, Metabolic Diseases, Molecular Biology, Neuroendocrinology, Primary Cell Culture, Protein Purifications, Quantitative Assay, Target Validation Preferred Skills: G Protein-Coupled Receptors (GPCRs), High-Throughput Screening Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only: Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics. As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities. For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit: EEOC Know Your Rights EEOC GINA Supplement We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another’s thinking and approach problems collectively. Learn more about your rights, including under California, Colorado and other US State Acts The sa
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