Senior Director, Global Regulatory Affairs – Biotech Unit

BeiGene, Ltd.; Northern (KY); Hybrid; USD 211,000 - 281,000; Full time

Benefits offered by this job

Medical

Dental

Vision

401(k)

FSA/HSA

Life Insurance

Paid Time Off

Wellness

Job summary

BeOne Medicines Ltd. seeks a seasoned Regulatory Affairs Lead to drive global regulatory strategies for development programs in oncology. You will oversee regulatory aspects from preclinical through lifecycle management, coordinating with advisory committees and execution units to ensure compliant, timely submissions.

Required: 12+ years in biotech/pharma, 5+ years in leadership, and extensive FDA interactions. Travel up to 20% and strong collaboration across geographies are essential.

Qualifications

• Bachelor’s degree required; advanced degree preferred.
• Minimum 12 years in biotech/pharma with 5+ years in regulatory leadership.
• Experience leading regulatory programs across multiple geographies (US, EU, Asia).

Responsibilities

• Provide high-level regulatory direction for development programs across phases.
• Lead preparation and submission of IND/CTA, NDA/MAA across global markets.
• Interface with Health Authorities to expedite approvals and manage issues.
• Mentor Execution Unit and ensure study planning aligns with regulatory strategy.
• Develop and implement regulatory processes and risk assessments.

Skills

Regulatory leadership

Global regulatory strategy

Regulatory submissions

FDA interactions

Oncology knowledge

Education

Bachelor’s degree

Advanced degree preferred

Tools

Microsoft Office

Job description

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer.

General Description

At BeOne, our Global Development SuperHighway — our integrated, end-to-end, wholly internal development capability — is a cornerstone of our R&D vision. It brings together a unique set of internal cross‑functional capabilities from across the globe needed for efficient delivery of clinical trials to develop impactful medicines to accelerate access to innovation for patients around the world. We are now opening this same delivery engine to the world’s most promising external science. Through SuperHighway partnerships, highly promising assets from leading biotech partners can access our development capabilities creating a true win‑win ecosystem with the ultimate goal of helping more patients around the world. This is not a fee‑for‑service model; it is a bold new way to grow the company and expand what’s possible in oncology. This is a rare opportunity to help build something genuinely new — joining a high-caliber, agile team at the leading edge of clinical development innovation. If you are energized by building, by challenging the status quo, and by making a real impact on patients’ lives, this is where you belong.

Role Overview

The position contributes to the overall partnership program strategy and driving its vision and mission. Leveraging deep therapeutic and functional area expertise, the Regulatory Affairs Lead is accountable for developing, implementing, and advising on global regulatory strategies for development programs to secure and maintain market access for products in line with the partnership program’s goals, and in coordination with key Advisory Committee and Execution Unit. The Lead manages all regulatory aspects of allocated assets through all phases of development, post-approval, and lifecycle of the product. The incumbent will provide leadership and strategic regulatory oversight for designated projects ensuring that the latest requirements and standards are met. This role helps deliver the partnership studies that run on our Clinical SuperHighway, supporting seamless onboarding and high‑quality execution of external partner projects in close partnership with the execution functions.

Essential Functions of the Job

Accountable for providing high level strategic and operational regulatory direction and mentorship on projects including, but not limited to general regulatory strategies, regulatory requirements for clinical studies and marketing approval in multiple countries, regulatory strategic development plans and risk assessments, critical issue management and advice on Health Authority interactions. Use extensive knowledge of US, China, EU and ICH regulatory requirements and the ability to apply knowledge both strategically and operationally to allocated assets. Oversee the preparation and submission of documentation to support investigational and marketing registration packages throughout the world and ensures timelines are met. Review sections of IND/CTA, NDA/MAA/NDS, and other global submission documents in support of clinical trials and marketing applications, and their amendments in conformance with local regulatory requirements. Liaise and negotiate with global regulatory authorities as needed for all aspects pertaining to drug development including resolution of key regulatory issues and to expedite approvals of product and labeling changes. Maintain awareness of global regulatory environment and assess impact of changes on business and product development programs. Facilitate policy and development of standard interpretation of global regulation. Integrates functional expertise with business knowledge to solve problems and make good decisions for the overall business. Manages critical issues, taking leadership for the regulatory contribution. Responsible for assisting with the development and implementation of regulatory processes. Consult with Advisory Committee for relevant topics and incorporate the ideas into strategy and execution if appropriate. Provide guidance to Execution Unit at regional and global level and ensure timely, quality, and efficient study planning and execution of associated clinical studies. Conduct regular review meetings with Execution Unit to mentor, support, and ensure all studies are tracking to quality and timeline. Report on study status, goals, operational KPIs, and enforce quality KPIs. Champions a global mindset and approach across GRA to foster collaboration and consistency across the organization. Participate company-wise standard discussion, finalization, and implementation. Other duties as assigned.

Supervisory Responsibilities

N/A (individual contributor role; no direct reports).

Education Required

Bachelor’s degree required; advanced degree preferred. A minimum of 12 years in the biotechnology or pharmaceutical industry and a minimum of 5 years in a regulatory leadership capacity with a broad background in oncology.

Computer Skills

Skilled in Microsoft Office Suite

Other Qualifications

Experience of working as a lead in Regulatory Affairs across two or more major geographic areas, and experience of leading multiple FDA interactions for oncology products leading to Agency approval actions. Experience should clearly be demonstrative of managerial, leadership, and collaboration ability across multiple functional areas. Thorough understanding of drug development process, the pharmaceutical industry and healthcare environment including regulatory requirements and policy trends. Extensive regulatory experience with INDs/CTAs, NDAs/BLAs/MAAs, lifecycle management, interactions with Health Authorities, developing, and implementing regulatory strategies with a proven track record of significant regulatory accomplishments. Very strong strategic skills including creativity and effectiveness in identifying and addressing major strategic challenges and the ability to balance short‑term needs with long‑term vision. Proven ability to deliver on goals within a cross‑functional team/partnership environment with a high level of professionalism. Excellent interpersonal skills and the ability to build and maintain positive work relationships to effectively interface at all levels across the organization. Fluent in written and verbal English. Desirable: knowledge of Mandarin.

Desirable

knowledge of Mandarin.

Travel

Up to 20%. Ability to travel domestically and internationally.

Global Competencies

• Fosters Teamwork
• Provides and Solicits Honest and Actionable Feedback
• Self-Awareness
• Acts Inclusively
• Demonstrates Initiative
• Entrepreneurial Mindset
• Continuous Learning
• Embraces Change
• Results-Oriented Analytical Thinking/Data Analysis
• Financial Excellence
• Communicates with Clarity

Salary Range

Salary Range: $211,200.00 - $281,200.00 annually

BeOne is committed to fair and equitable compensation practices. Actual compensation packages are determined by several factors that are unique to each candidate, including but not limited to job-related skills, depth of experience, certifications, relevant education or training, and specific work location. Packages may vary by location due to differences in the cost of labor. The recruiter can share more about the specific salary range for a preferred location during the hiring process. Please note that the listed range reflects the base salary or hourly range only. Non-Commercial roles are eligible to participate in the annual bonus plan, and Commercial roles are eligible to participate in an incentive compensation plan. All Company employees have the opportunity to own shares of BeOne Medicines Ltd. stock because all employees are eligible for discretionary equity awards and to voluntarily participate in the Employee Stock Purchase Plan.

• Medical
• Dental
• Vision
• 401(k)
• FSA/HSA
• Life Insurance
• Paid Time Off
• Wellness

We are proud to be an equal opportunity employer.

BeOne does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans’ Readjustment Assistance Act of 1974, Title I of the Americans with Disabilities Act of 1990, and any other applicable federal, state or local laws, applicants who require reasonable accommodation in the job application process may contact [e-mail].

BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide. With a broad portfolio, we are expediting development of our diverse pipeline of novel therapeutics through our internal capabilities and collaborations. We are committed to radically improving access to medicines for far more patients who need them.

Our growing global team of more than 11,000 colleagues spans six continents.

To learn more about BeOne, please visit www.beonemedicines.com and follow us on LinkedIn, X (formerly known as Twitter), Facebook and Instagram. For more information, please visit the link to explore job opportunities in China Mainland.

China Mainland Job Posting At BeOne

how we work is just as important as the work we do. Below are our Values that determine the decisions we make and how we do things.

• Patients First
• Driving Excellence
• Bold Ingenuity
• Collaborative Spirit