Senior Clinical PM – Oncology (Onsite, San Diego)

Regulatory Jobs

San Diego (CA)

On-site

USD 120,000 - 160,000

Full time

5 days ago
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Benefits offered by this job

Industry-leading pay
Company-paid healthcare
Flexible spending accounts
Voluntary life insurance
401K matching
Uncapped vacation

Job summary

Iambic Therapeutics is seeking an experienced Senior Project Manager to lead cross-functional planning and execution of clinical drug development programs. This on-site role at our San Diego Headquarters requires coordinating multiple workstreams and external partners to meet study milestones and deliverables.

The ideal candidate has 7+ years of PM experience in pharma/biotech or 5+ years with a Master's, with oncology experience preferred and familiarity with Clinical Operations.

Qualifications

  • 7+ years of project management experience in the pharmaceutical/biotech industry or a Master’s with 5+ years.
  • Master’s degree with 5+ years experience is acceptable.
  • Oncology experience preferred.
  • Familiarity with regulatory submission processes.
  • Excellent organizational, communication, and interpersonal skills.

Responsibilities

  • Lead planning, execution, and tracking of project timelines and deliverables to align with milestones and company goals.
  • Oversee relationships with third-party vendors (e.g., CROs) and monitor scope, timelines, and performance.
  • Develop and maintain detailed project plans across development workstreams, including risk assessments and budget tracking.
  • Collaborate with Clinical Operations to track study timelines and critical path activities from start-up through execution.
  • Facilitate meetings by creating agendas, capturing decisions, and tracking action items.
  • Maintain accurate project documentation, including status reports and risk registers.
  • Monitor progress and implement mitigation strategies for risks, delays, or resource gaps.
  • Foster strong communication across Clinical Operations, Regulatory, Safety, Biostatistics, Data Management, CMC, and DMPK.

Skills

Cross-functional
Stakeholder management
Strong communication
Regulatory submissions

Education

Bachelor's degree in science/healthcare/business
Master's degree

Tools

Smartsheet
SharePoint
Confluence

Job description

Iambic Therapeutics is seeking an experienced Senior Project Manager to lead cross-functional planning and execution of clinical drug development programs. This on-site role at our San Diego Headquarters requires coordinating multiple workstreams and external partners to meet study milestones and deliverables.

The ideal candidate has 7+ years of PM experience in pharma/biotech or 5+ years with a Master's, with oncology experience preferred and familiarity with Clinical Operations.

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