Staff Scientist

* Train, mentor, and supervise laboratory personnel within the development subgroup, including instruction on new techniques, protocol adherence, and data integrity standards.
* Lead collaborative efforts to optimize proteomics methods, analytical modeling, and data interpretation across multidisciplinary and international partnerships.
* Serve as the primary contact for proteomics related collaborations, coordinating scientific priorities, troubleshooting technical challenges, and ensuring alignment with project objectives.
* Ensure compliance of all research activities with institutional, state, and federal regulatory requirements, including support for IRB protocols and human subject research standards.
* Serve as a scientific resource for data collection, experimental design, and complex data analysis, providing intellectual and technical expertise to advance project goals.
* Review and refine laboratory protocols, implement new methodologies, and manage complex, high dimensional research datasets.
* Lead and support scientific writing efforts, including preparation and revision of IRB protocols, peer reviewed publications, and federal and non federal grant submissions.
* Contribute to proofreading, fact checking, and scientific editing of manuscripts, grant applications, and professional presentations to ensure accuracy and clarity.
* Serves as a resource for collecting data and performing analysis. Contributes to facilitating and promoting a research project by providing scientific or intellectual information.
* Reviews laboratory protocols and training on new techniques. Manage complex data sets for research.
* Leads the contributions to scientific writing and publications, including protocols and grants.
* Performs other related work as needed.
* 3-5 years hands-on experience with LC-MS/MS systems strongly preferred.
* LC-MS/MS, bottom-up proteomics, sample preparation including working with plasma or tissue samples, bioinformatics/data analysis tools, and experimental design strongly preferred.
* Strong academic background with a publication record in peer-reviewed journals strongly preferred.
* Demonstrated knowledge in proteomics, mass spectrometry, cancer biology, translational research, or related scientific disciplines.
* Proficiency in advanced research methodologies, including proteomic workflows, experimental design, data acquisition, and quantitative analysis.
* Strong understanding of regulatory policies and procedures governing human subjects research, including IRB requirements and institutional compliance standards.
* Advanced analytical and critical thinking skills, with the ability to interpret complex, high dimensional datasets and translate findings into meaningful scientific conclusions.
* Proven problem solving skills, including the ability to troubleshoot experimental challenges, optimize methods, and refine analytical approaches.
* Exceptional attention to detail in experimental execution, data management, protocol development, and scientific documentation.
* Strong organizational skills, with the ability to manage multiple concurrent projects, collaborations, and regulatory timelines.
* Effective verbal and written communication skills, including the ability to contribute to manuscripts, grant applications, protocols, and professional presentations.
* Demonstrated ability to work both independently with minimal supervision and collaboratively within multidisciplinary and international research teams.
* Proficiency in Microsoft Office applications and familiarity with scientific data management and analysis platforms.
* Collaborative mindset with a commitment to advancing shared research goals while maintaining accountability for individual deliverables.
* Work is performed in a laboratory and research setting with routine exposure to biological specimens, chemicals, and standard laboratory equipment, in accordance with established safety protocols.
* Regular use of advanced proteomics and mass spectrometry instrumentation.
* Significant computer based work for data analysis, modeling, documentation, and scientific writing.
* Compliance with institutional safety standards, biosafety procedures, and regulatory requirements related to human subjects research.
* Ongoing collaboration with multidisciplinary research and clinical teams.
* Occasional schedule flexibility may be required to meet instrument availability and project deadlines.

When applying, the document(s)
** MUST
* * be uploaded via the
** My Experience
** page, in the section titled
** Application Documents
** of the application.

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