Director/Sr. Director, Head of Regulatory Affairs Policy, Intelligence and Data Transparency (Remote)

Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted protein degradation medicines, the next frontier in innovative drug design aimed at improving treatment options for patients with cancer and inflammatory diseases. Powered by a fully AI-integrated discovery engine capable of tackling any protein class, and coupled with unparalleled ligase expertise, Nurix’s dedicated team has built a formidable advantage in translating the science of targeted protein degradation into clinical advancements. Nurix aims to establish degrader-based treatments at the forefront of patient care, writing medicine’s next chapter with a new script to outmatch disease.

Job Summary:

Nurix Therapeutics, Inc. is seeking a Director/ Sr. Director, Head of Regulatory Affairs Policy, Intelligence and Data Disclosure and Transparency (DD&T) to join the Regulatory team.  The successful candidate will be a core member of the Regulatory team working in close collaboration with the VP, Head of Regulatory Affairs and other cross-functional colleagues. They will be a strong subject matter expert in regulatory processes, laws, and regulations, with a comprehensive understanding of how regulatory policy is shaped and developed with Europe and the US. The individual will also have extensive knowledge of clinical trial transparency regulations, track and inform about new DD&T requirements, developments, and latest updates as appropriate

This role will coordinate efforts in a highly collaborative cross-functional environment that addresses global policy & intelligence gathering, analysis of changes in the regulatory environment, coordination of policy positions and advocacy strategies to achieve policy goals, working collaboratively with both internal and external stakeholders to influence the policy environment set by global Health Agencies. This individual will work closely with RA colleagues to coordinate policies around the Nurix portfolio-assessing the impact of regulatory policy on products and goals.

Responsibilities:

• Coordinates and executes regulatory intelligence and policy strategies and operations to address current and future business needs in partnership with internal global, regional, and country level RA functions.
• Understands draft legislation, regulations, guidelines, and policies at the global level, and supports interactions and communications with trade associations and health authorities on regulatory policy matters relevant to organizational positions.
• Effectively supports Nurix’s positions and serve as a representative internally and externally on key policy topics to appropriately coordinate engagements within the regulatory environment as well as engage with medical societies and key industry trade associations.
• Provides insights and coordinate for global "one voice" positions on critical regulatory issues and trends to contribute to a broader policy platform.
• Coordinates the deployment of regulatory Intelligence resources and tools as well as access to them and provides focused regulatory insights to the RA organization and other stakeholders.
• Provides strategic expertise, possessing functional and soft skill to drive strategic intelligence and policy goals.
• In collaboration with regulatory writing, author and submit transparency submissions, including global clinical trial registrations, tabular results, plain language results summaries and/or performs document redactions throughout the study lifecycle in accordance with Nurix policy and international regulations
• Facilitates cross-functional team review and approval of transparency submissions on time and within compliance with regulatory and Nurix requirements
• Maintains and updates data disclosure tracking tools and dashboards to comply with applicable transparency requirements
• Participates in cross-functional process initiatives impacting regulatory submission processes and systems
• Manages consultants and contractors as needed

Experience and Skills:

• Bachelor's degree in life-sciences or related scientific discipline; advanced degree preferred
• Must have minimum of 12 years in Regulatory affairs experience with practical knowledge and expertise in Regulatory intelligence & policy with the EU and/or US.
• Proven capability in acting as a credible, influential, and respected spokesperson able to convey complex messages, trends & insights.
• Deep understanding of the regulatory environment and latest regulations and guidance’s with sound knowledge of intelligence tools and methods; preference will be given to candidates with therapeutic area experience (i.e., oncology).
• Strong relationship management and interpersonal skills