New · posted Nov 1
BeOne Medicines · Biotechnology
Director, Global Regulatory Project and Submission Management
- Remote, US
- Remote
- Full-time
- Director
The role
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: The Director, Global Regulatory Project Management (Director, Global RPM) is a senior strategic leader responsible for supporting, influencing, translating, and executing oncology regulatory strategies across the global drug development lifecycle. This role combines deep regulatory expertise with advanced project management and organizational leadership, driving successful NDA/BLA/MAA submissions and ensuring seamless cross-functional integration across regions. The Director, Global RPM proactively anticipates regulatory challenges, influences decisions, and champions process improvements to secure on-time submissions and maintain market access for products worldwide
Key Attributes
- Proactive, not reactive; knows the regulatory lifecycle and anticipates challenges and takes initiative to address them.
- Demonstrates integrity, accountability, and strategic leadership.
- Thrives in a global team environment and seeks excellence as the measure of success.
- Able to balance multiple tasks, prioritize effectively, and meet deadlines across time zones and regions.
What you need
Other Qualifications Experience
- Bachelor’s degree in Science or related discipline; advanced degree preferred.
- Minimum 10+ years of experience in regulatory project management and regulatory submissions, including both small molecules and biologics, with significant global exposure.
- Demonstrated experience in strategic regulatory leadership, with a proven track record of successful submissions and regulatory PM accomplishments in multiple regions.
- Experience leading cross-functional and cross-regional teams, influencing senior stakeholders globally.
- Strong business acumen, strategic thinking, and ability to integrate multiple sources of data for sound decision-making.
- Excellent verbal and written communication skills; able to understand and translate complex regulatory issues clearly to internal and external stakeholders worldwide.
- Skilled in conflict resolution, negotiation, and fostering open communication across cultures.
- PMP or similar certification preferred.
Global Competencies
When we exhibit our values of Patients First, Driving Excellence, Bold Ingenuity and Collaborative Spirit, through our twelve global competencies below, we help get more affordable medicines to more patients around the world.
- 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
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. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and Wellness.
Skills named in this posting
What you'll do
Strategic Global Leadership
- Support, translate, and implement global regulatory strategies for development programs, ensuring alignment with business objectives and long-term vision across all major regions (US, EU, China, APAC, LATAM, etc.).
- Serve as a principal advisor to the Global Regulatory Lead (GRL) and Regulatory Regional Leads (RRL), providing strategic regulatory oversight and recommendations for global product development, submissions, and lifecycle management.
- Integrate functional regulatory expertise with PM knowledge to solve complex problems and make sound decisions for the organization on a global scale.
- Maintain awareness of global regulatory environments, policy trends, and competitive landscapes, assessing impact and adapting strategies accordingly.
Global Project Management Excellence
- Lead and manage complex regulatory submissions (IND/CTA, NDA/BLA/MAA) across multiple regions, ensuring compliance with ICH, US, EU, China, and other international requirements.
- Act as the “COO” to the Global Regulatory Lead, translating strategic regulatory vision into actionable project plans, driving operational execution, and ensuring all cross-functional activities are coordinated and delivered on time.
- Organize and facilitate cross-functional meetings with global teams to coordinate, plan, and track submission activities, driving accountability and alignment among stakeholders worldwide.
- Proactively identify risks, propose solutions, and manage critical issues related to global regulatory submissions and strategy.
- Oversee preparation and submission of documentation to support investigational and marketing registration packages, ensuring timelines and quality standards are met globally.
Cross-Regional Collaboration
- Build partnerships with senior stakeholders and cross-functional teams (clinical, medical, safety, CMC, commercial) across regions to achieve strategic business goals through knowledge sharing and collaboration.
- Liaise and negotiate with cross-functional teams and regulatory authorities to expedite submission timelines and resolve key regulatory issues in all relevant markets.
- Mentor, guide, and develop junior and mid-level staff in project planning, regulatory processes, and professional development, fostering a global mindset.
Continuous Improvement
- Champion process optimization and improvement initiatives within the global regulatory PM function.
- Lead the development and implementation of regulatory processes and policies, fostering a culture of excellence and innovation across regions.
- undefined
Supervisory Responsibilities
- Proficiency with project management and document management tools, such as Smartsheets, MS Project, and Power BI.
- Advanced skills in the Microsoft Office suite (Word, Excel, PowerPoint, Outlook).
- Ability to quickly learn and adapt to new software platforms and digital collaboration tools.
- Experience with electronic document management systems and regulatory submission platforms is preferred.
Pay and benefits
$176,000 – $236,000 a year
Employer providedSalary Range: $176,000.00 - $236,000.00 annually
Medical, Dental, Vision
401(k)
FSA/HSA
Life Insurance
Paid Time Off
Annual bonus plan and equity awards
Working conditions
Travel
- Occasional international and domestic travel may be required to support global project teams, attend regulatory meetings, or participate in industry conferences.
- Travel requirements will vary based on project needs and organizational priorities.
Equal opportunity, accessibility and legal noticesBeOne Medicines's statements, word for word
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 [email protected].
Job intelligence
The context around this role
Live data · November 1, 2026
Salary intelligence
How the pay compares
This role's midpoint is 11% below the US median for Regulatory Affairs roles at this level.
This roleEmployer provided
Director roles in the US93 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $176,000 | — | $236,000 |
| All US (middle half) | $203,000 | $232,500 | $264,000 |
This role: BeOne Medicines's own published range. Comparisons: the base pay employers published on open Regulatory Affairs roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Regulatory Affairs
The general path across 298 open Regulatory Affairs roles on Regulatory Jobs, with the titles they carry most. Not BeOne Medicines's own promotion track.
Career resources on Regulatory Affairs
Skills DNA
What this role leans on
How many of the posting's 47 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Collaboration and leadership21
- Regulatory submissions10
- Documentation and SOPs4
- Data and digital systems2
- GMP and compliance1
- Lab testing and methods1
- Investigations and CAPA1
- Quality systems and risk1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
- ICHICH quality guidelines(official source, opens in a new tab)Q1 stability, Q2(R2) analytical validation, Q7, Q9 risk management, Q10 quality systems
- FDAFDA IND(official source, opens in a new tab)Investigational New Drug applications
- FDAFDA NDA(official source, opens in a new tab)New Drug Applications
- FDAFDA BLA(official source, opens in a new tab)Biologics License Applications
Company hiring pulse
BeOne Medicines on Regulatory Jobs
- 42
- Open roles
- 41
- Distinct roles
- 2
- Locations
By discipline
- Clinical21 50%
- Regulatory11 26%
- Quality9 21%
By level
- Director18 43%
- Manager11 26%
- Senior & Principal9 21%
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Director, Global Regulatory Project and Submission Management at BeOne Medicines
Open until filled. $176K–$236K a year, employer provided.