VP, Liver Development Asset Lead

Prime Medicine, Inc.

Cambridge (MA)

Hybride

USD 360 000 - 408 000

Plein temps

Il y a 6 jours
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Avantages offerts par ce poste

Comprehensive benefits package
401(k) match
Equity programs
Generous PTO and wellness days

Résumé du poste

Prime Medicine, Inc. in Cambridge, MA, is seeking an experienced Development Asset Leader to drive in vivo liver programs from IND clearance through regulatory approval.

You will lead a cross-functional team spanning Clinical, Regulatory, CMC, Biostatistics, and Medical Affairs, coordinating with CROs/CDMOs and KOLs while ensuring timelines, budget, and scientific rigor. The role grows into franchise leadership, scaling processes and governance to deploy capital across multiple assets.

Qualifications

  • Proven ability to lead multi-disciplinary programs across Clinical, Regulatory, CMC, and Nonclinical areas.
  • Experience directing liver/gene-editing or RNA-based programs is highly desired.
  • Experience with AI tools for project/portfolio management is a plus.

Responsabilités

  • Own the Integrated Development Plan for liver assets from IND acceptance through regulatory approval/licensure.
  • Frame critical considerations that change asset risk/value profile for executive teams.
  • Lead a matrixed team across Clinical, Regulatory, CMC, Biostatistics, Pharmacovigilance, Med Affairs, and Commercial.
  • Deploy AI-enabled project management tooling (timelines, risk registers, dashboards).
  • Design team structure, governance cadence, and knowledge-transfer for portfolio expansion.
  • Coordinate with CROs/CDMOs, KOLs, patient groups and Regulatory Affairs for asset interactions.

Connaissances

Cross-functional leadership
AI project management
Influence without authority
Strategic thinking
Executive communication

Formation

Advanced degree in life sciences/medicine

Description du poste

Prime Medicine, Inc. in Cambridge, MA, is seeking an experienced Development Asset Leader to drive in vivo liver programs from IND clearance through regulatory approval.

You will lead a cross-functional team spanning Clinical, Regulatory, CMC, Biostatistics, and Medical Affairs, coordinating with CROs/CDMOs and KOLs while ensuring timelines, budget, and scientific rigor. The role grows into franchise leadership, scaling processes and governance to deploy capital across multiple assets.

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