Associate Director Integrated Bioanalysis – Oncology Bioanalytical Project Lead

AstraZeneca

Cambridge, United Kingdom
Competitive salary; flexible employee benefits fun...
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Phd in immunology or related field
Regulated bioanalysis experience
Oncology portfolio leadership
** AstraZeneca is seeking an Associate Director for Integrated Bioanalysis focused on Oncology, based in Cambridge, UK. The candidate will lead bioanalytical strategy development and execution, collaborating with cross-functional teams to support drug development projects. **

Job Summary

  • This role involves spearheading the development and execution of comprehensive bioanalytical strategies to support AstraZeneca's innovative oncology pipeline.
  • The successful candidate will lead internal teams and external CROs while ensuring scientific oversight for preclinical and clinical studies.
  • AstraZeneca offers a competitive salary, flexible employee benefits fund, pension contributions, and a performance recognition scheme.

Matching Summary

Match Score: 75

** AstraZeneca is seeking an Associate Director for Integrated Bioanalysis focused on Oncology, based in Cambridge, UK. The candidate will lead bioanalytical strategy development and execution, collaborating with cross-functional teams to support drug development projects. **

Salary

Competitive salary; Flexible employee benefits fund; Pension contributions and Share Save Plans

Skills & Requirements

Must-have

  • PhD in immunology or related field
  • Regulated bioanalysis experience
  • Oncology portfolio leadership
  • Assay development and validation
  • CRO oversight and management
  • PK, PD, biomarker, and immunogenicity expertise

Nice-to-have

  • Matrix management experience
  • Mass spectrometry knowledge
  • Small molecule bioanalysis background
  • Publication and presentation record
  • Innovation and proactive learning

Key Requirements

  • PhD in immunology, biochemistry, biology, or related studies
  • Proven experience as Subject Matter Expert in regulated bioanalysis
  • Experience overseeing assay transfer and study conduct at CRO partners
  • Deep understanding of global regulatory expectations and guidance
  • Contributed to regulatory submission documentation such as INDs, NDAs, or BLAs

Work Rights

Not specified

Tailored Resume

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