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Clinical QA Specialist II, Clinical Specialist Providers (CSP)

Iovance Biotherapeutics · Remote

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Role summary

Iovance Biotherapeutics seeks a Clinical QA Specialist II to oversee clinical service provider qualification, compliance, and performance. The role involves managing CSP assessments, quality events, risk mitigation, and ensuring GCP compliance across multiple service categories.

What they're looking for

  • BS in life sciences or equivalent professional experience
  • 5+ years GCP or QA experience with 2+ years in service provider oversight
  • Strong written and oral communication skills
  • Exceptional organizational and critical thinking abilities
  • Ability to build partnerships and work diplomatically across departments
  • Proficiency with MS Office and relevant computer systems

What you'll be doing

  • Maintain CSP qualification and requalification programs using risk-based methodology
  • Conduct qualification activities for diverse service providers including CROs, labs, and imaging services
  • Identify and mitigate risks associated with CSP operations
  • Manage quality events, non-compliances, CAPAs, and negotiate quality agreements
  • Represent company at study management team and CSP meetings

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What RoleLantern checked

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RoleLantern checked active
RoleLantern checkedNeeds clarity
Date posted15 days ago
Last source check1 day ago
Salary listedNeeds clarity
Location clearClear
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