GSK·1 month ago
1 month ago
Director, Global Regulatory Affairs Lead (Oncology)
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What you'll do
- Develop and execute regulatory strategies for oncology assets, ensuring alignment with development plans and regulatory requirements.
- Lead cross-functional teams and provide regulatory leadership.
What they're looking for
- Experienced professionals in regulatory affairs within the pharmaceutical or healthcare industry.
Summarised by NextRaise from the employer’s description, which follows in full below.
Full description from employer
Become part of our team as Director, Global Regulatory Affairs Lead (Oncology), where you will develop and execute regulatory strategies for oncology assets, ensuring alignment with development plans and regulatory requirements. Lead cross-functional teams and provide regulatory leadership. Ideal for experienced professionals in regulatory affairs within the pharmaceutical or healthcare industry.
Skills
- regulatory strategy
- oncology regulatory affairs
- regulatory compliance
- health authority engagement
- regulatory intelligence
- regulatory precedent assessment
- cross-functional team leadership
- business resilience
- resource management
- communication
- stakeholder management
- digital fluency
- matrix leadership
- pharmaceutical regulatory compliance
- regulatory strategies
- regulatory due diligence
- portfolio assessment
- strategic recommendations
- regulatory matrix management
- business development support
- licensing support
- acquisition support
- regulatory risk assessment
- regulatory strategy development
- regulatory activity reporting
- regulatory policy development
- regulatory process improvement
- regulatory data analysis
- regulatory decision support
- regulatory compliance training
Company
GSK
Collegeville, United States of America
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