Senior Technical Program Manager - Preclinical, London

Isomorphic Labs

London, United Kingdom
On-site
Manage ind application process
Transition from discovery to development
Regulatory-compliant document management
You will play a pivotal role in operationalising our path to the clinic, managing the complex sequencing of our first IND submissions

Job Summary

  • You will play a pivotal role in operationalising our path to the clinic, managing the complex sequencing of our first IND submissions.
  • You will manage the timeline and sequencing of late-stage discovery including CMC, DMPK, pharmacology and tox reporting to enable successful submission, ensuring no critical path items are missed.
  • You will be the bridge between our scientific breakthroughs and regulatory reality, ensuring that our data management and documentation mature from research-grade to submission-ready standards.

Matching Summary

You will play a pivotal role in operationalising our path to the clinic, managing the complex sequencing of our first IND submissions.

Skills & Requirements

Must-have

  • manage IND application process
  • transition from discovery to development
  • regulatory-compliant document management
  • manage external vendors and collaborators
  • manage large budgets
  • sequencing complex multi-disciplinary activities

Nice-to-have

  • scientific background
  • formal program management qualification
  • high-growth Biotech or TechBio experience
  • experience with multiple modalities

Key Requirements

  • proven track record of managing an IND application process
  • deep experience at the intersection of discovery and early development
  • experience implementing or managing regulatory-compliant document management systems
  • experience working with external vendors and collaborators
  • experience managing large budgets
  • ability to manage complex schedules and logistics
  • high-level strategic input on regulatory hurdles

Work Rights

Not specified

Tailored Resume

Cover Letter