VP, Clinical Development

NewLimit

$200K — $250K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • M.D. or equivalent clinical training
  • Proven experience in first-in-human trial planning
  • Familiarity with US FDA and international regulatory agencies
  • Strong knowledge of Good Clinical Practices (GCP)
  • Experience in therapeutic areas related to metabolic and liver diseases preferred
  • Leadership experience in clinical development across multiple therapeutic areas
  • Background in emerging therapeutic modalities such as gene or cell therapies

Responsibilities

  • Lead and manage clinical development in partnership with external collaborators
  • Create and oversee clinical trial protocols and regulatory submissions
  • Address logistical challenges hindering clinical study progress
  • Contribute to budgeting and goal-setting as part of the Executive Team
  • Build and lead a clinical development team for first-in-human trials

Benefits

  • Health, dental, and vision insurance
  • 401(k) with company match
  • Generous paid time off policy -- 20 days/year plus holidays
  • Paid parental leave
  • On-site meals and snacks
Full Job Description
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
  • Experience with both US FDA and ex-US regulatory agencies (e.g. Australian TGA)
  • Deep knowledge of Good Clinical Practices (GCP)
Nice to have
  • Experience in metabolic and liver disease therapeutic areas
  • Experience leading a clinical development team across multiple therapeutic areas
  • Experience developing products in emerging therapeutic modalities (gene therapy, nucleic acid therapies, cell therapy)
  • Experience managing both early (Phase 1/2) and late-stage (Phase 3) clinical trials
Benefits
  • Health, dental, and vision insurance
  • 401(k) with company match
  • Industry-leading paid time off (PTO) -- 20 days/year for all employees + holidays
  • Paid parental leave
  • Meals and snacks on-site

Compensation for the role will depend on a number of factors, including a candidate's qualifications, skills, competencies, and experience. Learn more at: https://www.newlimit.com/careers

Similar Jobs

More Jobs at NewLimit

More Pharmaceuticals & Biotech Jobs

Find similar VP, Clinical Development jobs: