Associate Director Regulatory Policy and

vor 1 Woche

Zug, Schweiz Seagen Vollzeit

Seagen is a global, multi-product biotechnology company dedicated to developing and commercializing transformative cancer medicines. As the industry leader in antibody-drug conjugate (ADC) technology, we pioneered a new generation in the science of harnessing antibodies to deliver cell-killing agents directly to cancer cells. Seagen’s dedication to improving the lives of cancer patients goes beyond science, and we believe that every employee has a role in contributing to this mission. By working together with a shared dedication and diverse perspectives, we are able to reach our full potential and make a real difference in the world. Seagen is a fast-growing company and has an abundance of opportunities available for you to grow your career. Put your passion to work at Seagen and join us

Summary:
The Associate Director, Regulatory Policy & Intelligence, will be responsible for conducting regulatory intelligence gathering, consolidation and communication activities to support global product teams. They will support external regulatory intelligence and advocacy activities as an engaged member of trade and professional associations and be responsible for the development and maintenance of knowledge management processes and systems to maximize impact of regulatory intelligence on product strategy.

Principal Responsibilities
- Supports RLs & GRLs in providing up-to-date regulatory intelligence including responses to Ad hoc requests
- Defines and oversees the standardization and implementation of systems/processes to monitor the regulatory environment for changes that may have an impact on Seagen’s products and company goals
Anticipates changes in the regulatory environment and identifies opportunities to influence change
- Ensures effective communication of evolving regulatory expectations and requirements and the organization’s regulatory readiness activities to relevant leadership and governance bodies
- Collaboratively develops and maintains knowledge management strategies related to regulatory intelligence
- Identifies strategic opportunities and ensure organizational contribution to and participation on pertinent committees and other regulatory forums
- Manages trade association and consortium engagements; acts as Seagen representative to trade and industry organizations in support of business needs

Qualifications:

- 7-10 years’ experience in life sciences including 5+ years’ experience in regulatory affairs, preferably in regulatory strategy or intelligence. Oncology experience desirable
- Deep understanding of European regulations and guidance governing drugs and biologics in all phases of development, including post-marketing, with a good understanding of basic regulatory requirements in Canada, US and emerging markets
- Excellent collaboration and relationship building skills
- Outstanding written and oral communication skills.
- Proven ability to work with a high level of integrity, accuracy, and attention to detail
- Ability to work in a cross-functional team environment
- Strong attention to detail and the ability to handle multiple tasks
- Excellent organizational, computer and documentation skills and an ability to prioritize effectively
- thorough understanding of local compliance, as well as a sound ethical approach to business

**Education**:

- Bachelor’s degree or equivalent in data science or the life sciences. BA/BS accepted based on experience. Advanced degree preferred-
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