Associate Director, Oncology Diagnostics CDx

Gilead Sciences Inc.

Maryland

On-site

USD 196,000 - 253,000

Full time

14 days+
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Benefits offered by this job

Medical insurance
Dental insurance
Vision insurance
Life insurance
Discretionary stock-based incentives
Paid time off

Job summary

Gilead Sciences Inc. is seeking a senior diagnostic leader to define CDx strategies for oncology programs and oversee integrated diagnostic plans across global regions.

You will lead cross-functional teams, coordinate biomarker objectives with clinical plans, and provide SME support to drug development teams. The role requires 10+ years in science with oncology diagnostics, strong leadership, and a track record in regulatory engagement.

Qualifications

  • Experience developing diagnostic strategies for oncology programs.
  • Ability to align biomarker hypotheses with clinical development plans.
  • Familiarity with diagnostic regulatory requirements and CRO oversight.

Responsibilities

  • Represent the diagnostic function on global program teams.
  • Lead Diagnostic Sub Teams and co-lead diagnostic partner teams.
  • Develop, articulate, and manage integrated diagnostic project plans with stakeholders.
  • Collaborate with biomarker, regulatory, clinical development, and operations teams.
  • Work independently in a fast-paced matrix environment to align resources.

Skills

Diagnostic strategy development
Oncology biomarker expertise
Cross-functional leadership
Clinical study design
Regulatory knowledge
Scientific communication

Education

BA/BS in a scientific discipline
MA/MS
MD or PhD

Tools

IHC
NGS
Flow cytometry
Digital pathology

Job description

Gilead Sciences Inc. is seeking a senior diagnostic leader to define CDx strategies for oncology programs and oversee integrated diagnostic plans across global regions.

You will lead cross-functional teams, coordinate biomarker objectives with clinical plans, and provide SME support to drug development teams. The role requires 10+ years in science with oncology diagnostics, strong leadership, and a track record in regulatory engagement.

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