Remote Biotech Project Manager - Oncology & Immunotherapy

Diakonos Oncology Corp.

United States

Remote

USD 120,000 - 180,000

Full time

5 days ago
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Job summary

Diakonos Oncology Corp. is seeking an experienced biotech Project Manager to turn cross-functional decisions into coordinated execution.

The role spans clinical, CMC, regulatory, preclinical, and research, with hands-on accountability and clear action ownership. You’ll work to keep milestones, risks, and recovery actions visible via dashboards and status updates, coordinating with CROs, CDMOs, and academic partners.

Qualifications

  • Bachelor’s degree in healthcare or another scientific discipline (or equivalent).
  • 5+ years of clinical project management experience.
  • Hands-on PM experience in biotech, pharma or a related life-sciences setting.
  • The confidence to hold colleagues and senior leaders accountable while keeping working relationships constructive.
  • Clear writing and speaking, with sound judgment about when to resolve an issue yourself and when to escalate.

Responsibilities

  • Own the integrated project plan across clinical, CMC, regulatory, preclinical, and research.
  • Turn leadership decisions and meeting outcomes into clear actions with owners and due dates, and follow through until they’re done.
  • Identify critical-path activities, dependencies, and tradeoffs, and bring options to leadership.
  • Coordinate handoffs with internal teams, CROs, CDMOs, and academic partners.
  • Run focused project reviews and keep action and decision logs.
  • Keep milestone progress, risks, and recovery actions visible through dashboards and status updates.

Education

Bachelor’s degree in healthcare or scientific discipline
5+ years of clinical project management experience
Hands-on PM experience in biotech/pharma/life sciences

Tools

Asana
Microsoft 365/SharePoint

Job description

Diakonos Oncology Corp. is seeking an experienced biotech Project Manager to turn cross-functional decisions into coordinated execution.

The role spans clinical, CMC, regulatory, preclinical, and research, with hands-on accountability and clear action ownership. You’ll work to keep milestones, risks, and recovery actions visible via dashboards and status updates, coordinating with CROs, CDMOs, and academic partners.

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