Director Public Policy - Science and Food and Drug Administration Policy
Regeneron
August 12, 2026
Remote friendly (Washington, DC)
United States
Corporate Functions
Director of Policy & Government Affairs – Science and FDA Policy
Responsibilities:
- Lead Regeneron’s science and FDA policy portfolio; develop, shape, and influence policy related to biopharmaceutical R&D and cell and gene therapy across the product lifecycle.
- Engage internal experts to identify policy risks/opportunities and set short- and long-term policy objectives.
- Communicate Regeneron’s policy positions and initiatives to internal and external audiences.
- Organize and participate in events, conferences, and forums to promote the policy agenda.
- Represent the PP&GA team at key stakeholder meetings; engage external partners to identify collaboration opportunities.
- Collaborate with alliance development lead to build coalitions with industry associations, advocacy groups, and other stakeholders.
- Develop and advance strategic public policy positions aligned to business objectives.
- Monitor and analyze legislative and regulatory developments (federal, state, local, and international) and assess impact on Regeneron.
Qualifications:
- Bachelor’s degree required; advanced degree(s) in Public Policy, Political Science, Law, or related field and science background strongly preferred.
- Minimum 12 years of relevant experience in science and regulatory policy; preferably substantial US FDA experience.
- Proven record crafting and influencing public policy; ability to navigate complex, highly technical issues.
- Strong understanding of biopharmaceutical regulatory and legislative processes.
- Experience developing and executing strategic advocacy plans, including crafting/vetting legislative and regulatory proposals.
- Provide expert guidance on policy and regulatory matters to internal stakeholders.
Responsibilities:
- Lead Regeneron’s science and FDA policy portfolio; develop, shape, and influence policy related to biopharmaceutical R&D and cell and gene therapy across the product lifecycle.
- Engage internal experts to identify policy risks/opportunities and set short- and long-term policy objectives.
- Communicate Regeneron’s policy positions and initiatives to internal and external audiences.
- Organize and participate in events, conferences, and forums to promote the policy agenda.
- Represent the PP&GA team at key stakeholder meetings; engage external partners to identify collaboration opportunities.
- Collaborate with alliance development lead to build coalitions with industry associations, advocacy groups, and other stakeholders.
- Develop and advance strategic public policy positions aligned to business objectives.
- Monitor and analyze legislative and regulatory developments (federal, state, local, and international) and assess impact on Regeneron.
Qualifications:
- Bachelor’s degree required; advanced degree(s) in Public Policy, Political Science, Law, or related field and science background strongly preferred.
- Minimum 12 years of relevant experience in science and regulatory policy; preferably substantial US FDA experience.
- Proven record crafting and influencing public policy; ability to navigate complex, highly technical issues.
- Strong understanding of biopharmaceutical regulatory and legislative processes.
- Experience developing and executing strategic advocacy plans, including crafting/vetting legislative and regulatory proposals.
- Provide expert guidance on policy and regulatory matters to internal stakeholders.