Scientist II/Sr. Scientist I, In-Vivo Pharmacology (Must Have Immunology Experience)

• PhD. in Immunology, Pharmacology, or a related discipline
• 3+ years of industry experience with expertise in mouse models of autoimmune disease
• Strong foundation in translational immunology, including experience designing and executing in vivo studies
• Experience in biomarker assay development, cytokine profiling, immune-cell characterization, scRNAseq, flow cytometry, and preparing human biospecimen samples
• Proven ability to analyze complex biological data and communicate findings clearly
• Strong organizational skills and attention to detail
• Excellent interpersonal and communication skills with a collaborative mindset
• Ability to manage multiple priorities and deliver high-quality results in a fast-paced environment
• Track record of scientific achievement, including publications or impactful project contributions

We are seeking a highly motivated and experienced immunologist to join our In Vivo Pharmacology team at the Scientist or Senior Scientist level. This individual will play a critical role in designing, executing, and interpreting in vivo studies in immunology, with a particular emphasis on mouse models of autoimmune disease.

The successful candidate will contribute across multiple discovery-stage programs through IND-enabling studies, working closely with cross-functional partners in biology, medicinal chemistry, and DMPK. This role is ideal for a scientifically rigorous and collaborative individual who thrives in a fast-paced, innovative environment.

• →Design, plan, and execute in vivo pharmacology studies in mouse models of autoimmune disease
• →Analyze, interpret, and present complex datasets to multidisciplinary project teams and senior leadership
• →Collaborate cross-functionally with biology, medicinal chemistry, and DMPK teams to inform study design and data interpretation
• →Maintain accurate, detailed, and timely experimental records in electronic lab notebooks (ELN)
• →Contribute to study reports, regulatory documentation, and scientific publications as needed