The role involves developing and validating assays to identify and characterize small molecule mitochondrial uncouplers for treating metabolic diseases. The scientist will design screens, analyze mechanisms of action, and publish findings in peer-reviewed journals.
At Lilly, the work is demanding because patients are waiting.
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The Molecular Pharmacology group in Lilly Small Molecule Discovery (LSMD) and Cardiometabolic research unit (CMR) is seeking an ambitious post-doctoral scientist with strong research and communication skills to contribute to highly visible research projects.
Your work will focus on establishing and applying assays to evaluate mitochondrial uncouplers in a context- and system-dependent manner, and on screening for novel small molecule uncouplers with potential to treat metabolic disease.
In this role, you will: Develop and validate assays to identify small molecule uncouplers.
Characterize in vitro mitochondrial uncoupling activity across cell types, tissues, and disease-relevant systems.
Work with and be mentored by experts in bioenergetics, molecular pharmacology, and metabolic disease biology.
Design and execute small molecule screens to identify novel mitochondrial uncouplers, and characterize their mechanism of action, potency, selectivity, and safety margin using cutting edge industry technology and resources.
Identify areas of key need across clinical development and champion creative solutions to address those needs.
Maintain external awareness and learning to benefit the organization.
Present findings at conferences and publish in high quality peer-reviewed journals.
Basic Qualifications Ph.D. in Molecular Biology, Biochemistry, Cell Biology, Pharmacology, or a related field Qualified applicants must be authorized to work in the United States on a full-time basis.
Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.
Additional Skills/Preferences Demonstrated hands-on experience with molecular biology techniques, including CRISPR/Cas9 gene editing (e.g., guide RNA design, generation of knockout/knock-in cell lines, validation of edits) Experience with plate-based assay technologies such as TR-FRET, BRET, AlphaLISA, or similar high-throughput biochemical/cellular assay platforms preferred Familiarity with cellular target engagement assays (e.g., CETSA, NanoBRET target engagement, or similar approaches) preferred Experience with cell-based imaging techniques, including high-content/high-throughput imaging, fluorescence microscopy, or confocal imaging, for applications such as target engagement, phenotypic profiling, or trafficking studies Proficiency in RT-PCR/qPCR techniques for gene expression analysis Experience with proteomics and/or chemical biology approaches (e.g., mass spectrometry-based proteomics, activity-based protein profiling, chemical probe development) is a plus Strong scientific communication skills and a record of peer-reviewed publication.
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Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.
Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $58,000 - $123,200 Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees. #WeAreLilly
A Ph.D. in Molecular Biology, Biochemistry, Pharmacology, or a related field is required. Candidates must have hands-on experience with molecular biology techniques and be authorized to work in the US without sponsorship.
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Market context
In Indiana, post-doctoral scientist roles in molecular pharmacology are typically driven by research programs in universities, academic medical centers, and biotech settings that need advanced lab expertise. Competition is often strongest for candidates with a Ph.D., hands-on molecular biology experience, and U.S. work authorization, since those qualifications closely match the core requirements. Review the original posting carefully and confirm your technique experience aligns with the lab’s methods; this platform AI-summarizes requirements and benefits from the source description, saving you research time.
