Microbiology Research Program Sr. Specialist

University of Chicago•Chicago, IL

9d•$100,000 - $140,000•Onsite

About The Position

The Microbiology Research Program Senior Specialist supports and advances complex microbiology research programs under the direction of the Principal Investigator (PI), with an emphasis on vaccine development and translational research. This role leads the execution of research projects, aligns technical milestones with program goals, and ensures all activities meet rigorous standards of scientific quality and regulatory compliance. The Senior Specialist independently performs and oversees highly technical laboratory work, implements standardized protocols, and ensures the accuracy, reliability, and validity of team-generated data. As a cross-functional subject matter expert, this position provides guidance on best practices, troubleshoots complex experimental challenges, and translates research findings—spanning vaccine candidates, antigen discovery, immune response characterization, and assay development—into actionable insights for product, clinical, or public health applications. This position is well-suited for an experienced microbiology professional who combines deep technical expertise in microbiology and vaccine-related research with strong programmatic, regulatory, and communication skills. This at-will position is wholly or partially funded by contractual grant funding which is renewed under provisions set by the grantor of the contract. Employment will be contingent upon the continued receipt of these grant funds and satisfactory job performance.

Requirements

PhD in related field.
7+ years of work experience in a related job discipline.

Nice To Haves

7+ years in vaccine development and conducting advanced microbiology research in an academic, clinical, or industry setting.
Demonstrated proficiency in designing, executing, and troubleshooting complex microbiology experiments and assays.
Experience implementing and maintaining standardized laboratory protocols, quality control procedures, and data management practices.
Familiarity with relevant regulatory frameworks and biosafety requirements; experience working under IBC oversight.
Proven ability to analyze, interpret, and present complex scientific data.
Strong written and oral communication skills, including experience contributing to grants, manuscripts, and scientific presentations.
Demonstrated ability to work collaboratively in cross-functional teams and to provide technical guidance to other research staff.

Responsibilities

Assist the PI by directing the execution of microbiology research programs and aligning technical milestones with overall program goals, including projects focused on vaccine discovery, optimization, and evaluation.
Manage high-impact research initiatives, including those related to vaccine development (e.g., antigen selection, formulation studies, immunogenicity assessments), ensuring projects are delivered on time, within scope, and to high scientific standards.
Implement and oversee quality assurance of research performed by others to guarantee the accuracy, reliability, and validity of data, particularly for studies informing vaccine candidate selection and preclinical evaluation.
Implement standardized protocols and manage data to prevent errors across all pre-analytical, analytical, and post-analytical phases of a study.
Provide guidance on best practices and input into protocol development for microbiology and vaccine-related methods, including assay validation and optimization relevant to vaccine research.
Troubleshoot complex laboratory challenges and interpret test results; investigate and recommend alternative approaches to improve the quality and consistency of results across microbiology and vaccine development workflows.
Independently perform a wide range of highly technical and complex research and laboratory tests and procedures, including those relevant to evaluating vaccine candidates (e.g., in vitro and ex vivo models, pathogen characterization, immune readouts).
Ensure all research operations follow applicable regulatory standards (e.g., FDA, ISO, cGMP), where relevant to microbiology and vaccine-development activities.
Oversee biosafety practices, laboratory equipment maintenance, and laboratory documentation to support compliance and audit readiness for studies involving pathogens and vaccine candidates.
Enforce Institutional Biosafety Committee (IBC) protocols and ensure adherence to institutional and regulatory guidelines, including those applicable to vaccine-related research.
Serve as a cross-functional subject matter expert for other research personnel and institutional partners.
Analyze experimental data and translate research findings into actionable products, clinical, or public health applications, including informing vaccine candidate advancement, assay transfer, or clinical trial readiness.
Interface with R&D, clinical affairs, regulatory, and commercial teams to ensure alignment between laboratory research, vaccine development strategies, and downstream applications (e.g., preclinical packages, regulatory submissions, translational studies).
Assist the PI by drafting, editing, and proofreading funding proposal documents; prepare written materials, figures, charts, and graphs on specialized techniques and research results for peer-reviewed scientific publication or presentation, including vaccine-related findings (e.g., immunogenicity, efficacy, mechanistic studies).
Present research findings at national and international academic conferences and symposia, including meetings focused on vaccines, infectious diseases, and translational microbiology.
Uses specialized depth and breadth of expertise to lead and conduct research experiments.
Interprets and collects data and trains others in the interpretation of data. Leads the dissemination of data and significantly contributes to scientific publications and grant writing.
Leads others to solve complex problems, providing expertise to the team which includes of scientists and clinicians from the University and nationally.
Provides expertise to identify protocol problems, inform investigators of problems, or assist in problem resolution efforts, such as protocol revisions. Provides expertise to evaluate factors such as sample collection processes, data management plans, or potential subject risks.
Performs other related work as needed.