We’re looking for a highly execution-focused, hands-on Scientist in Pharmacology to contribute to cardiovascular and metabolic disease programs, particularly in obesity and MASH. This position is well suited for an MS-level scientist with 10+ years of relevant experience who brings strong bench expertise and can independently lead both in vitro, cell-based mechanistic studies and in vivo rodent PK/PD work—delivering complete, high-quality data packages to advance pipeline programs. Experience with RNA or oligonucleotide therapeutics is a plus but not required. What matters most is demonstrated excellence in hands-on pharmacology. If you have a solid track record running metabolic in vitro assays and conducting rigorous in vivo mouse studies, the team can provide training on RNA/oligonucleotide-specific approaches and workflows.
Responsibilities
Study Ownership & Execution
- Design and execute integrated in vitro and in vivo studies aligned with project goals
- Analyze and interpret data to generate clear, decision-ready insights
- Present results and recommendations to project teams
- Manage timelines, identify risks, and troubleshoot effectively
In Vitro Pharmacology (Oligonucleotides)
- Perform ASO/siRNA delivery and transfection
- Conduct dose-response and time-course studies to assess target engagement, potency, and functional outcomes
- Evaluate assay performance, including off-target and cytotoxicity effects
Metabolic Cell Biology & Assays
- Culture and maintain relevant cell models (e.g., hepatocytes, myotubes, adipocytes)
- Run assays related to lipid metabolism, insulin sensitivity, and energy balance
- Perform lipid accumulation, glucose uptake, mitochondrial function, and biomarker assays
Molecular Biology
- Perform qPCR/RT-qPCR, Western blotting, and ELISA/Luminex assays
- Support RNA/protein workflows and data interpretation
In Vivo Pharmacology (Rodent Studies)
- Design and execute mouse studies (lean and DIO models)
- Conduct PK/PD, dose-response, and metabolic assessments (e.g., GTT, ITT, metabolic cages)
- Collect and process blood/tissue samples for downstream analysis
- Ensure compliance with IACUC protocols and animal welfare standards
Data Analysis & Compliance
- Analyze data using standard tools (e.g., Prism, Excel) and apply appropriate statistics
- Maintain accurate documentation and data integrity (ELN)
- Prepare reports and presentations for internal stakeholders
- Ensure compliance with institutional SOPs and regulatory guidelines
Required Skills
- Master’s degree in Life Sciences, Pharmacology, Biomedical Sciences, or a related discipline
- 10+ years of hands-on experience across metabolic in vitro models/assays and rodent in vivo pharmacology, including dosing and tissue collection
- Proven ability to independently design, execute, analyze, and report studies
- Experience authoring and obtaining approval for IACUC protocols (beyond simply following them)
- Strong attention to experimental rigor, including proper controls, thorough documentation, reproducibility, and data integrity
- Effective collaborator with clear communication skills and a strong translational science mindset
- Experience with RNA-based approaches (siRNA/ASO) is a plus, but not required; training can be provided for candidates with solid metabolic and in vivo pharmacology expertise
SGD 58,*************,000