Full-Time

Executive Director / Vice President, Biology & Translational Pharmacology

Profluent

Profluent

51-200 employees

AI-designed bespoke proteins for genetic therapies

Compensation Overview

$270k - $340k/yr

+ Equity participation + 401(k) employer match

No H1B Sponsorship

Emeryville, CA, USA

In Person

PhD, MD

Category
Biology & Biotech (1)
Required Skills
Pharmacology

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Requirements
  • An advanced degree such as a PhD, MD, DVM, PharmD, or equivalent in pharmacology, molecular biology, genetics, physiology, hepatology, bioengineering, medicine, or a related discipline.
  • At least 12 years of biopharmaceutical research and development experience for a PhD in a related discipline.
  • A strong track record in genetic medicines, liver biology, translational pharmacology, and preclinical development.
  • A demonstrated track record advancing multiple therapeutic programs from concept through development candidate nomination.
  • Deep experience with genetic medicines or advanced therapeutic modalities such as RNA interference, antisense oligonucleotides, messenger RNA/lipid nanoparticles, gene therapy, genome editing, or related platforms.
  • Deep understanding of liver biology and metabolic disease, including connecting human genetics, disease biology, pharmacology, biomarkers, translational models, and development strategy.
  • Extensive experience with rare liver diseases, lipid biology, hepatology, fibrosis biology, and/or metabolic liver disease.
  • Experience designing and interpreting in vivo pharmacology studies in rodent and/or non-human primate models, including pharmacokinetics/pharmacodynamics, biodistribution, dose response, target engagement, pharmacodynamic biomarkers, durability, efficacy, and tolerability.
  • Demonstrated ability to lead multidisciplinary scientific teams, including direct management of senior scientists or functional leaders and leadership of matrixed drug-discovery project teams.
  • Working knowledge of investigational new drug-enabling requirements, toxicology interfaces, chemistry, manufacturing, and controls considerations, bioanalytical assay needs, and regulatory expectations sufficient to guide program-level decisions.
  • The ability to tailor scientific and strategic messages for technical project teams, senior executives, board members, external advisors, partners, and generalist investors.
  • Direct experience or high-level familiarity with gene-editing proteins such as nucleases, base editors, prime editors, and recombinases.
Responsibilities
  • Build and oversee a liver biology and translational pharmacology organization, including directly managing program and in vivo pharmacology leaders.
  • Lead scientific strategy and execution for two to three liver-directed genetic medicine programs.
  • Provide accountable leadership for cross-functional therapeutic program teams integrating translational biology, genome editing, protein engineering, delivery, pharmacology, bioanalytics, chemistry, manufacturing, and controls, regulatory, and preclinical development expertise.
  • Partner with functional leaders to define program resourcing, critical-path activities, timelines, risks, and key experiments required to deliver development candidates and investigational new drug-ready data packages.
  • Guide in vivo pharmacology strategy across rodent and non-human primate studies, including model selection, dose strategy, biodistribution, editing activity, durability, target engagement, pharmacodynamic biomarkers, tolerability, and translational relevance.
  • Apply liver and metabolic disease expertise to experimental design across genetically defined disease contexts.
  • Apply scientific judgment to experimental design, data interpretation, and program decision-making to support clear go/no-go decisions.
  • Translate the liver portfolio vision into actionable program strategy and contribute to prioritization of additional genetically defined opportunities in liver and other tissues.
  • Represent program strategy, data, risks, and recommendations to executive leadership, board members, external advisors, potential partners, investors, and collaborators.
  • Cultivate a collaborative, execution-oriented culture while maintaining scientific rigor, prioritization, and high standards for data quality.
Desired Qualifications
  • Experience advancing at least one program into investigational new drug-enabling studies or clinical development is strongly preferred.

Profluent.bio designs custom proteins for genetic medicines using artificial intelligence. Its core offering is bespoke protein solutions tailored to therapeutic needs for pharmaceutical and biotech partners, helping advance treatments for genetic diseases. The product works by applying AI to optimize protein design, effectively decoding the “language of life” to create proteins that extend beyond natural or existing patented options. Partners collaborate on projects, with revenue coming from upfront fees, milestones, and royalties on successful commercialization of therapies that use their proteins. The company differentiates itself by combining AI-driven protein design with a partnership model in the gene editing and synthetic biology space, aiming to deliver more effective and precise treatments while enabling cost-efficient development. The goal is to accelerate genetic medicine by providing optimized proteins that enable new or improved therapies for genetic diseases.

Company Size

51-200

Company Stage

Late Stage VC

Total Funding

$149M

Headquarters

Emeryville, California

Founded

2022

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Simplify Jobs

Simplify's Take

What believers are saying

  • Lilly's April 28, 2026 pact promises up to $2.25 billion plus royalties.
  • Profluent raised $106 million, bringing total funding to $150 million for model expansion.
  • Tens of thousands accessed OpenCRISPR-1, strengthening distribution and partner credibility in 2025.

What critics are saying

  • Lilly controls selected recombinases exclusively, forcing Profluent into partnership dependence after April 2026.
  • Open-source OpenCRISPR-1 invites commoditization, weakening pricing power and partner urgency by 2027.
  • If kilobase-scale recombinases fail in vivo, Profluent becomes a research shop, not a medicines company.

What makes Profluent unique

  • Profluent designs proteins from scratch, not by editing existing natural scaffolds.
  • OpenCRISPR-1, released in 2025, validated AI-designed genome editing in human cells.
  • Its Protein2PAM models and CRISPR-Cas Atlas speed enzyme discovery across modalities.

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Benefits

Health Insurance

Unlimited Paid Time Off

Growth & Insights and Company News

Headcount

6 month growth

1%

1 year growth

-1%

2 year growth

7%
AI Software Services
May 5th, 2026
Unlocking AI innovation in finance medicine and music.

Unlocking AI innovation in finance medicine and music. Published on May 05, 2026 GENETIC MEDICINE REVOLUTION: AI AND BIOTECH JOIN FORCES. In a groundbreaking partnership, Lilly and AI-driven Profluent Bio are teaming up in a deal worth up to $2.25 billion to develop advanced DNA editing tools. Their goal? To create precise treatments for genetic conditions that currently lack effective solutions, using innovative AI models to design enzymes that can target multiple mutations in the genome. This collaboration aims to unlock the "holy grail" of genetic medicine through kilobase-scale DNA editing. This matters because it could transform how AI Software Services treat genetic diseases, offering hope to millions who suffer from conditions deemed untreatable. The tools being developed are likely to be accessible, lowering barriers to entry in a field that has traditionally been expensive and exclusive. Imagine a startup that provides a platform for creators and developers to access these AI-driven genetic editing tools, enabling them to innovate and create personalized therapies. This could attract investors eager to support the next wave of medical breakthroughs!

Pharmaceutical Technology
Apr 29th, 2026
Eli Lilly bets on recombinases in $2.25bn Profluent R&D pact.

Eli Lilly bets on recombinases in $2.25bn Profluent R&D pact. The pair will harness AI to discover and develop recombinases for precise, large-scale gene editing. Eli Lilly is locking down on its rapid expansion strategy with a second deal this week - joining forces with artificial intelligence (AI) biotech, Profluent, to develop recombinases for large-scale gene editing. The deal, which will see Lilly hand over an undisclosed upfront payment and funding for Profluent's R&D efforts, could deem the biotech eligible for $2.25bn in development and commercial milestones. Profluent will also see tiered royalties on net sales if any of the developed recombinases were to make it to market. Through this partnership, Lilly and Profluent will work across multiple programmes, which will focus on developing and commercialising site-specific recombinases for diseases with "severe unmet needs". To achieve this, Profluent will take an AI-driven approach - using the technology to create and optimise custom recombinases targeting exact locations in the genome to enable large-scale, precise DNA editing. Under the deal's terms, Lilly will also gain the exclusive rights to take selected recombinases through both early and clinical development to commercialisation. According to Profluent, altering DNA on a kilobase scale could help address the variation in mutations often seen across patients with genetic diseases - potentially allowing more patients in a heterogeneous population to gain benefit compared with the one-size-fits-all approach taken by standard knock-out and base editing methods. In a statement, Profluent's co-founder and CEO, Ali Madani, noted that kilobase-scale DNA editing is the "holy grail in genetic medicine," and AI is the only way to truly unlock the potential of designer recombinases for any location in the genome. Lilly forges on with dealmaking spree. Lilly's partnership with Profluent is not the big pharma's first foray into the world of recombinases, as the company previously forged a $1.12bn collaboration with German biotech, Seamless Therapeutics, to develop recombinase-based therapies for hearing loss in January 2026. The Indiana-based pharma, alongside Johnson & Johnson, also poured funds into an $85m financing raised by in vivo gene editing startup, Stylus Medicine - supporting the development of its cancer therapies. Alongside its activity in the recombinase space, Lilly has been on somewhat of a dealmaking spree over the first months of 2026, having handed over $21bn to acquire six biotechs across operating areas like oncology, immunology and cardiovascular diseases. Most recently, the pharma company bought Janus kinase (JAK) inhibitor specialist, Ajax Therapeutics, for $2.3bn - potentially expanding its presence in the blood cancer market. Lilly's deal-heavy strategy is similarly mirrored across the pharmaceutical space, as companies look to restock their pipelines amid the looming patent expiries facing their portfolios. Give your business an edge with its leading industry insights.

Tech in Asia
Apr 29th, 2026
Eli Lilly signs $2.3B AI gene-editing deal with Profluent to develop DNA medicines

Eli Lilly has signed a deal worth up to $2.25 billion with Profluent, an AI biotech startup, to develop DNA-editing medicines using AI-designed proteins called recombinases. The partnership gives Lilly exclusive rights to any resulting medicines, though upfront fees and disease targets were not disclosed. The collaboration focuses on inserting kilobase-scale DNA sequences into specific genome locations, aiming to surpass CRISPR/Cas9's capabilities. Profluent CEO Ali Madani described this as the "holy grail" of genetic medicine. The deal extends Lilly's AI drug discovery push, following a $1.12 billion agreement with Seamless Therapeutics in January. Profluent also released OpenCRISPR-1, an open-source AI-generated gene editor that matched SpCas9's efficiency whilst reducing unintended edits by 95% in human cell tests.

Business Wire
Nov 19th, 2025
Profluent Raises $106M to Scale Frontier AI Models for Programmable Biology

Profluent, a leader in frontier AI for protein design, today announced a $106 million financing co-led by Altimeter Capital and Bezos Expeditions, with parti...

Bionews, Inc.
Nov 19th, 2025
Partners to design AI-based gene editing therapies for Rett

Partners to design ai-based gene editing therapies for Rett. The Rett Syndrome Research Trust (RSRT) is teaming up with Profluent Bio to use artificial intelligence (AI) to design personalized gene-editing therapies for Rett syndrome. Profluent will leverage its AI tools to engineer molecules that can correct mutations in the MECP2 gene, the most frequent cause of Rett syndrome. RSRT has awarded Profluent $1 million to fund the partnership. "Our AI is built to navigate a vast design space and find solutions that are out of reach with manual protein engineering methods, resulting in personalized mutation-specific genomic medicines that are an ideal match for each Rett patient," Peter Cameron, PhD, Profluent's senior vice president of gene editing and translation, said in a company press release. "Together with RSRT, we're excited to turn progress in the lab into impact for patients." Rett syndrome is caused mainly by mutations in the MECP2 gene, resulting in less production of a working protein with the same name that plays an important role in brain development and communication between brain cells. Gene editing tools, such as CRISPR/Cas9, are used in research and clinical settings to remove, add, or modify pieces of DNA with the goal of treating genetic diseases. Focusing on mutation. Base editing uses modified versions of the CRISPR system to make precise changes to a single building block (nucleotide) in the MECP2 gene. Profluent said its AI models will be used to develop base editors that target mutations often found in Rett syndrome patients. Profluent will initially focus on the T158M mutation, which changes the amino acid sequence in the MeCP2 protein from threonine to methionine. Amino acids are the proteins' building blocks. The new editors will fit inside a harmless adeno-associated virus (AAV) and make room for systems that prevent them from accidentally causing edits in the brain beyond the intended one. "This collaboration is about people first - Rett families are trusting us with a challenge that affects them 24/7," said Hilary Eaton, PhD, chief business officer at Profluent. "Profluent is committed to using AI as the equalizer and democratizing the field of gene editing; whether a patient has a rare or common disease, they deserve access to safe, high-quality treatments." The company presented data on Protein2PAM, an AI, deep learning model capable of engineering Cas proteins that could be used to develop customized base editors for Rett, at the Rett Syndrome Genetic Medicines Summit, held in September in Boston. "Families in our community face seizures, loss of speech, and profound disability," said Monica Coenraads, CEO of RSRT. "They are counting on us to push the science forward. We believe Profluent's frontier AI can accelerate the development of custom editing solutions for our patients with serious unmet medical need." Last year, RSRT launched a program, Roadmap to Cures, aimed at raising $40 million to bring three genetic medicines to clinical trials by 2028. Andrea Lobo, PhD Andrea Lobo holds a PhD in cell biology/neurosciences from the University of Coimbra-Portugal, where she studied stroke biology. As a research scientist for 19 years, Andrea participated in academic projects in multiple research fields, from stroke, gene regulation, cancer, and rare diseases. She has authored multiple research papers in peer-reviewed journals.