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Jobs / Regulatory Affairs Specialist in United States of America
2 months ago
GSK·2 months ago
2 months ago

Associate Director Regulatory Affairs, Oncology

Collegeville, United States of AmericaFull-timeSenior · 10-15 yearsRegulatory Affairs Specialist

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Top 10% of NextRaise users matched against Regulatory Affairs Specialist roles in United States.

Must-have skills for this role

  • regulatory strategy development
  • oncology regulatory affairs
  • regulatory strategies
  • drug development process

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About this role

Seeking an Associate Director Regulatory Affairs, Oncology to develop and execute global and regional regulatory strategies for oncology assets. Lead regulatory interactions, ensure compliance, and collaborate with cross-functional teams. Ideal for experienced professionals in regulatory affairs with expertise in oncology and regulatory strategy.

Skills

  • regulatory strategy development
  • oncology regulatory affairs
  • drug development process
  • regulatory submissions
  • regulatory strategy implementation
  • matrix leadership
  • pharmaceutical regulatory compliance
  • regulatory strategies
  • business resilience
  • resource management
  • stakeholder management
  • communication
  • digital fluency
  • clinical trial requirements
  • licensing requirements
  • regulatory intelligence assessment
  • competitive analysis
  • problem solving
  • continuous improvement
  • oncology research
  • regulatory agency interaction
  • early medicine development
  • medication profile development
  • labeling development
  • matrix working
  • creative regulatory problem-solving
  • network development

Company

GSK
Collegeville, United States of America

Company facts come from this company's own listings. We only show what the postings themselves carry.

Sourced from GSK·first seen 31 Aug 2026·last verified 8 Sept 2026·How we source jobs

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