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VP, Clinical Development

NewLimit - South San Francisco, CA

Posted Apr 8, 2026

Benefits

Parental leave
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Non-birth-parent leave
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Family-building benefits
  • Fertility benefits: Not verified
  • Adoption assistance: Not verified
  • Surrogacy assistance: Not verified
Mental health support
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Relocation assistance
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Childcare support
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Learning budget
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Verification
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Salary
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401(k) match
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Market context

U.S. role benchmark (BLS OEWS)
$81,444 U.S. median for this role
Projected growth (BLS Employment Projections)
+6.9% - Faster than average

Matched to SOC 29-1141 - Healthcare aggregate by role bucket.

Source: U.S. Bureau of Labor Statistics, OEWS, May 2024 and Employment Projections, 2024-2034.

Role

Role function
Healthcare From the posting source checked Jun 20, 2026
Seniority
Senior From the posting source checked Jun 20, 2026

Schedule

Shift type
Not verified
Weekend work
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Company

Company stage
Early From the posting source checked Jun 20, 2026

Application

Cover letter
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Assessment
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Deadline
Not stated

Where they hire

State eligibility is not yet verified.

About this role

VP, Clinical Development South San Francisco, CA Company info NewLimit is a biotechnology company working to radically extend human healthspan. We're developing medicines to treat age-related diseases by reprogramming the epigenome, a new therapeutic mechanism to restore regenerative potential in aged and diseased cells. We leverage functional genomics, pooled perturbation screening, and artificial intelligence systems to unravel the biology of aging and disease using experiments of unprecedented scale. Description NewLimit is recruiting a VP of Clinical Development to plan and execute our first clinical trials. Our most advanced assets restore youthful hepatic metabolism and hold the potential to benefit diverse populations with liver disease and metabolic dysfunction. Our early stage programs have similar potential for impact in renal and inflammatory disease indications. In this role, you will design and orchestrate clinical trials for some of the world's first reprogramming medicines. You will serve as the company's senior clinical scientist and as a member of our executive team. As part of your role, you will: - Lead and orchestrate clinical development activities in collaboration with external partners. - Create clinical trial protocols, author and own regulatory submissions, and contribute to regulatory interactions. - Solve the inevitable logistical bottlenecks that block progress of our clinical studies. - Serve as a member of NewLimit's Executive Team and contribute to budgeting, goal setting, and technical review decisions. - Build and run a clinical development team as we approach first-in-human dosing. Requirements - M.D. or equivalent clinical training - Experience planning and orchestrating first-in-human trials

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