SereNeuro Therapeutics

Chief Science Officer

Founding-team-level translational Chief Scientific Officer role owning the scientific direction of the company and serving as its external scientific face. The role focuses on setting scientific vision, strategy, and pipeline prioritization, driving SN101 from preclinical proof-of-concept through IND-enabling development to first-in-human, and building and leading the science organization.

Key Responsibilities
  • Scientific vision, strategy & prioritization across platform and pipeline, including portfolio and stop/go decisions.
  • Starting material & line strategy: genomic stability, off-target/edit characterization, immunogenicity, GMP banking, provenance/consent, freedom-to-operate.
  • Potency & characterization: define and validate a potency-assay strategy for SN101's dual mechanism (sequestration + reparative secretome)
  • Nonclinical package: own the tumorigenicity / residual-undifferentiated-cell / malignant-transformation strategy expected of any pluripotent-derived product; biodistribution; pharmacology; GLP toxicology.
  • Regulatory science: co-author INTERACT, pre-IND, and IND strategy; lead the RMAT and accelerated-approval scientific narrative with the CEO.
  • External scientific voice: lead the scientific story for investors (co-lead the Series A), pharma partners, conferences, and KOLs/SAB, including our sports-medicine and military-medicine key opinion leaders.
  • Team & culture: recruit, mentor, and lead the science team; set scientific standards and rigor.
Required
  • PhD and/or MD with deep translational experience in iPSC-derived cell therapy.
  • Has personally led at least one program from preclinical through IND, ideally into clinical development.
  • Was on the science/leadership team of a company that raised a Series A or later.
  • Loves to pitch publicly. Demonstrated excellence and genuine enthusiasm as a scientific presenter to investors, on the conference stage, and with KOLs; comfortable being the company's scientific face.
  • Working fluency in cell-therapy CMC and regulatory expectations: potency assays, tumorigenicity/residual pluripotency, genomic stability, comparability, biodistribution, and CBER/Office of Therapeutic Products interactions.
  • Track record building and leading scientific teams.
Preferred
  • Prior military service or elite/professional athlete, to anchor credibility, networks, and mission resonance in our pro-athlete and military-medicine beachhead markets.
  • Domain depth in pain / sensory neuroscience (DRG, nociceptor biology), osteoarthritis / musculoskeletal & joint biology, and/or immunomodulation / secretome-based therapeutics.
  • iPSC differentiation toward neural / sensory lineages.
  • Experience with RMAT / accelerated-approval programs.
  • Prior CSO or Head/VP-Research scope at a seed- or Series A-stage cell-therapy company, or experience as a scientific co-founder.

About SereNeuro

SereNeuro develops advanced therapies for pain. Our lead program, SN101, is a first-in-class iPSC-derived, pain-sensing neuron therapy delivered by intra-articular injection for chronic osteoarthritis (OA) joint pain. SN101 is a “living, multi-channel pain sponge” that both sequesters inflammatory pain mediators and secretes a reparative secretome (halting cartilage loss and remodeling subchondral bone). SN101 is analgesic and disease-modifying, validated to date in ex vivo human tissue and in murine and large-animal models, with durable, joint localized engraftment.


The Role

We are hiring a founding-team-level translational Chief Scientific Officer to own the scientific direction of the company and be its external scientific face. You will set scientific vision, strategy, and pipeline prioritization; drive SN101 from preclinical proof-of-concept through IND-enabling development to first-in-human; co-lead the Series A as our lead scientific presenter; and build and lead the science organization. You will report to the CEO and work alongside our scientific co-founders/advisors and Senior Principal Scientist (Cell Therapy), who reports to you.


What You'll Lead

Drive preclinical pipeline to IND, partnering with CMC

  • Scientific vision, strategy & prioritization across platform and pipeline, including portfolio and stop/go decisions.
  • Starting material & line strategy: genomic stability, off-target/edit characterization, immunogenicity, GMP banking, provenance/consent, freedom-to-operate.
  • Potency & characterization: define and validate a potency-assay strategy for SN101's dual mechanism (sequestration + reparative secretome)
  • Nonclinical package: own the tumorigenicity / residual-undifferentiated-cell / malignant-transformation strategy expected of any pluripotent-derived product; biodistribution; pharmacology; GLP toxicology.
  • Regulatory science: co-author INTERACT, pre-IND, and IND strategy; lead the RMAT and accelerated-approval scientific narrative with the CEO.
  • External scientific voice: lead the scientific story for investors (co-lead the Series A), pharma partners, conferences, and KOLs/SAB, including our sports-medicine and military-medicine key opinion leaders.
  • Team & culture: recruit, mentor, and lead the science team; set scientific standards and rigor.


Required

  • PhD and/or MD with deep translational experience in iPSC-derived cell therapy.
  • Has personally led at least one program from preclinical through IND, ideally into clinical development.
  • Was on the science/leadership team of a company that raised a Series A or later.
  • Loves to pitch publicly. Demonstrated excellence and genuine enthusiasm as a scientific presenter to investors, on the conference stage, and with KOLs; comfortable being the company's scientific face.
  • Working fluency in cell-therapy CMC and regulatory expectations: potency assays, tumorigenicity/residual pluripotency, genomic stability, comparability, biodistribution, and CBER/Office of Therapeutic Products interactions.
  • Track record building and leading scientific teams.


Strongly Preferred

  • Prior military service or elite/professional athlete, to anchor credibility, networks, and mission resonance in our pro-athlete and military-medicine beachhead markets.
  • Domain depth in pain / sensory neuroscience (DRG, nociceptor biology), osteoarthritis / musculoskeletal & joint biology, and/or immunomodulation / secretome-based therapeutics.
  • iPSC differentiation toward neural / sensory lineages.
  • Experience with RMAT / accelerated-approval programs.
  • Prior CSO or Head/VP-Research scope at a seed- or Series A-stage cell-therapy company, or experience as a scientific co-founder.
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