Associate Director, Analytical Development And Vendor Management

Sanabiotech

Cambridge, MA, United States
Base: $170,000 to $210,000pyear; bonus/equity: not...
On-site
Phd with 5+ years experience or equivalent
Hands-on analytical assay development
Experience managing outsourced cro work
This role bridges discovery-stage science with downstream development needs by combining hands-on lab work with scientific leadership of outsourced activities

Job Summary

  • This role bridges discovery-stage science with downstream development needs by combining hands-on lab work with scientific leadership of outsourced activities.
  • The successful candidate will design, develop, and optimize analytical assays while serving as the primary scientific interface with CRO partners to ensure data quality and comparability.
  • Sana Biotechnology offers a comprehensive benefits package including health coverage, paid time off, 401(k) matching, and tuition reimbursement to support employee wellness and career growth.

Matching Summary

This role bridges discovery-stage science with downstream development needs by combining hands-on lab work with scientific leadership of outsourced activities.

Salary

Base: $170,000 to $210,000/year; Bonus/Equity: Not specified; Benefits: Generous health coverage, PTO, 401(k) match, tuition reimbursement

Skills & Requirements

Must-have

  • PhD with 5+ years experience or equivalent
  • Hands-on analytical assay development
  • Experience managing outsourced CRO work
  • Molecular and biochemical methodologies expertise
  • Assay qualification and validation experience
  • GCP compliant environment experience

Nice-to-have

  • Regulatory BioA environment experience
  • Clinical development and site management background
  • Fast-paced dynamic working environment adaptability
  • Mentoring and leading diverse teams
  • Strong communication skills for cross-functional stakeholders

Key Requirements

  • PhD required with 5+ years experience
  • Bachelor's or MS with 8+ years experience
  • 4+ years in analytical development within biotech/pharma
  • Experience in GCP compliant environments
  • Proven track record managing CROs

Work Rights

Not specified

Tailored Resume

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