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Retro Biosciences

Project Manager - Preclinical & Translational Programs

1w

Retro Biosciences

Redwood City, US · Full-time · $170,000 – $230,000

About this role

Retro develops therapies for diseases driven by the biology of aging, focusing on cellular reprogramming and autophagy to add 10 years to healthy human lifespan. We're building a mission-driven team embracing startup culture of rapid iteration, transparency, and versatility. We seek an experienced Project Manager to support cell therapy programs advancing toward IND-enabling and IND submission milestones.

As Project Manager, you'll work with deeply technical teams on ambitious problems, enabling strong execution, alignment, and decision-making. You'll ensure complex scientific, manufacturing, and regulatory workstreams move forward efficiently and on time. You're a builder of clarity, creating structure from ambiguity with crisp plans, owners, timelines, and next actions.

You'll operate across pre-clinical science, translational strategy, manufacturing, and regulatory teams, translating between languages and constraints. You track details so scientists can focus on what matters, surfacing risks early and resolving blockers with a calm, low-ego, mission-first approach. Coordinate with internal scientists, CMC leads, regulatory stakeholders, and external vendors like CDMOs and CROs.

Drive direct impact on programs approaching the clinic by hitting milestones without sacrificing quality. Maintain momentum with lightweight documentation like timelines, decision logs, and risk registers. Support leadership in portfolio reviews and resource allocation across programs.

Requirements

  • Bachelor’s degree in life sciences, engineering, or a related field
  • 5+ years of project or program management experience in biotech, pharma, or a closely related life sciences environment
  • Hands-on experience supporting pre-IND and/or IND-enabling programs
  • Working knowledge of cell therapy drug development workflows, including research, CMC, and regulatory interfaces
  • Experience managing external vendors and cross-functional teams
  • Strong organizational skills and a demonstrated ability to drive accountability
  • Clear, concise communicator who can work effectively with scientists and technical stakeholders

Responsibilities

  • Drive project management for preclinical and translational programs, focusing on IND-enabling activities and transition into clinical development
  • Build and maintain integrated program plans spanning research, CMC, regulatory, and external partners
  • Track timelines, dependencies, risks, and decision points across cross-functional teams
  • Coordinate closely with internal scientists, CMC leads, regulatory stakeholders, and external vendors (CDMOs, CROs, consultants)
  • Ensure manufacturing and regulatory timelines stay aligned with scientific plans
  • Monitor and support follow-through on cross-disciplinary action items, deliverables, and commitments
  • Maintain clear, lightweight documentation (timelines, decision logs, risk registers)
  • Support leadership by preparing materials for portfolio reviews and identifying resource constraints