Clinical Program Director, IND-to-Trial (AI-Driven)

Isomorphic Labs

Cambridge (MA)

On-site

USD 140,000 - 210,000

Full time

10 days ago

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Job summary

Isomorphic Labs in Cambridge, MA is seeking an Associate Director of Clinical Program Management to steer programs from IND through clinical trial execution, guiding cross-functional teams and external partners to deliver on milestones using AI-enabled approaches.

Reporting to the Program Lead, you will manage timelines, budgets, risks, and vendor relationships, while maintaining speed, quality, and regulatory readiness across multiple therapeutic areas.

Qualifications

  • Proven track record managing a clinical program from IND to late-stage development.
  • Experience coordinating cross-functional teams and external vendors.
  • Strong budgeting and schedule management across interdependent timelines.
  • Ability to operate in a fast-paced environment with a sense of urgency.
  • Excellent leadership and communication skills; able to motivate diverse groups.

Responsibilities

  • Develop and own integrated clinical program plans from IND to trials.
  • Lead cross-functional clinical trial teams and ensure alignment.
  • Lead project team meetings and ensure effective information sharing.
  • Collaborate with preclinical, AI/ML, and data science teams to accelerate execution.
  • Oversee external vendors, CROs, and partners with budgets and timelines.
  • Provide regular updates to leadership on study execution and portfolio.
  • Proactively identify issues that affect deliverables and budgets.

Skills

Clinical program management
Cross-functional leadership
Budget and timeline management
Risk management
Urgency and accountability
Adaptability
Leadership and communication
Vendor collaboration

Job description

Isomorphic Labs in Cambridge, MA is seeking an Associate Director of Clinical Program Management to steer programs from IND through clinical trial execution, guiding cross-functional teams and external partners to deliver on milestones using AI-enabled approaches.

Reporting to the Program Lead, you will manage timelines, budgets, risks, and vendor relationships, while maintaining speed, quality, and regulatory readiness across multiple therapeutic areas.

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