David N. Primer

Eli Lilly · Boulder, Colorado

David N. Primer, Ph.D.

Director, CMC Process Chemistry

Senior process chemistry leader translating discovery-stage oncology programs into scalable, GMP-ready manufacturing routes.

Portrait of David N. Primer, Ph.D.

About

Process chemistry, end to end.

I lead CMC process chemistry teams that develop, optimize, and scale the synthetic routes behind oncology drug candidates — moving programs from gram-scale discovery deliveries through hundred-kilogram GMP manufacture.

My work sits at the intersection of synthetic invention, crystallization and form control, vendor and tech-transfer management, and the practical realities of clinical-supply timelines. Earlier in my career I co-developed the photoredox / nickel dual-catalysis cross-coupling strategy that opened up C(sp2)–C(sp3) bond formation as a routine pharmaceutical disconnection.

Peer-reviewed publications
15
Patents
3
Largest GMP scale led
>400 kg
Direct reports mentored
8

Education

  • University of Pennsylvania

    2012 – 2017

    Ph.D., Organic Chemistry

    GPA 3.97 / 4.00 · Advisor: Prof. Gary A. Molander · Thesis: Single-Electron Transmetalation: Radical-Mediated Alkyl Transfer in Cross-Coupling.

  • Emory University

    2008 – 2012

    B.S., Chemistry

    GPA 3.37 / 4.00 · Undergraduate research with Prof. Huw M. L. Davies on chiral silver and gold carbenoid reactivity.

Industry experience

Selected roles

  1. Eli Lilly

    Director, CMC Process Chemistry

    2022 – present

    Boulder, CO

    • Lead and develop the CMC process chemistry team — coordinating project assignments, technical training, and career development.
    • CMC project lead for LSN4170130, coordinating across three external vendors, discovery partners, and the broader CMC development team.
    • Developed the 4-step GMP route for LY4050784, internally delivering 500 g for GLP tox on an accelerated timeline; the process has since scaled to >100 kg at multiple GMP vendors.
    • Developed the 5-step GMP route for LY3866288 and led tech transfer activities that cut timelines by 70% and costs by 50% — keeping Phase 1 plans on pace for accelerated approval; scaled to >400 kg externally.
  2. Bristol Myers Squibb

    Senior Scientist / Principal Scientist, Chemical Process Development

    2020 – 2022

    New Brunswick, NJ

    • Optimized the final three steps of the CC-94676 (BMS-986365) synthesis — delivering >12 kg of Phase 1 material as racemate and as both single diastereomers in high chemical and enantiomeric purity.
    • Managed and trained two scientists on process development and route scouting toward a key intermediate in the bifunctional degrader portfolio.
    • Identified multiple crystalline forms of a high-MW (>900) greasy API, enabling the program to transition from amorphous precipitation to a controlled crystallization.
    • Provided technical leadership for tech transfers to partner sites in Colorado, Wisconsin, India, and China.
    • Co-designed browser-based high-throughput-experimentation software with ACD Labs and internal IT, improving data capture across the solubility, catalysis, and class-variable screening groups.
  3. Celgene Corporation

    Scientist I / II, Drug Substance Development

    2017 – 2020

    Summit, NJ

    • Developed a crystallization-induced resolution of a racemic amine — providing the first commercial-scale access to the single-enantiomer of a glutarimide-containing scaffold.
    • Scaled three processes from 500 g to >20 kg, supporting on-site manufacturing in Switzerland, the United Kingdom, and the United States for the synthesis of Iberdomide.
    • Filed a patent application and published a peer-reviewed paper on the novel processes developed for CC-90010.

Selected publications

Peer-reviewed work.

Fourteen peer-reviewed publications and two issued patents, with co-authorship in Nature, Science, JACS, Nature Protocols, and OPRD. Click any cover to read the article.

Citation counts and the full bibliography are tracked on Google Scholar.

Contact

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