Sr. Manager, Biobank

Amgen Australia Pty Ltd

Base: $137,365.95 - $185,848.05 usd; bonus/equity:...
Not specified
Doctorate degree phd pharmd or md
3-8 years industry experience in clinical trials
Expertise in biospecimen management and biobanking
Amgen Australia is seeking a Senior Manager for Biobank operations to support clinical programs and enhance productivity in biospecimen management. The ideal candidate should possess significant experience in clinical trials, informed consent regulations, and project management within the pharmaceutical or diagnostic sectors

Job Summary

  • This role involves serving as the senior escalation authority for complex informed consent and biospecimen governance matters while partnering with Institutional Review Boards.
  • The position requires leading a multi-layered operating model across internal staff and FSP partners to drive operational performance and cost efficiency.
  • Amgen offers a comprehensive benefits package including retirement plans, health coverage, stock-based incentives, and flexible work models.

Matching Summary

Match Score: 85

Amgen Australia is seeking a Senior Manager for Biobank operations to support clinical programs and enhance productivity in biospecimen management. The ideal candidate should possess significant experience in clinical trials, informed consent regulations, and project management within the pharmaceutical or diagnostic sectors.

Salary

Base: $137,365.95 - $185,848.05 USD; Bonus/Equity: Discretionary annual bonus and stock-based long-term incentives; Benefits: Comprehensive health, dental, vision, retirement plan, and flexible time-off

Skills & Requirements

Must-have

  • Doctorate degree PhD PharmD or MD
  • 3-8 years industry experience in clinical trials
  • Expertise in biospecimen management and biobanking
  • Knowledge of GCP ICH FDA guidelines
  • Experience with informed consent regulations

Nice-to-have

  • Strong project management skills
  • Experience navigating matrixed organizations
  • Excellent verbal and written communication
  • Collaborative internal and external relationships
  • Critical thinking and organizational skills

Key Requirements

  • PhD, PharmD, or MD required
  • Master's degree with 6 years experience OR Bachelor's with 8 years
  • 7+ years work experience in clinical research setting preferred
  • Knowledge of Laboratory Information Management Systems (LIMS)
  • Working knowledge of document management applications like Veeva

Work Rights

Not specified

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