Associate Director, Regulatory Affairs

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: BeOne is seeking an experienced and energetic person to manage, evaluate, and complete regulatory projects consistent with company goals. This individual will be responsible for developing, implementing, and advising on regulatory strategies for development programs to secure and maintain market access for product(s) in line with business objectives, and in coordination with key internal & external stakeholders. Furthermore, the incumbent will have regulatory accountability for assigned programs, working with other members of the regulatory team to ensure high-quality, timely completion of regulatory deliverables. This individual will provide leadership and strategic regulatory guidance to teams for designated projects ensuring the latest requirements, standards, and trends within the company and industry are met. The Associate Director will also manage regulatory aspects of compounds through all phases of development, post-approval, and life-cycle commitments. The individual will interface with regulatory Health Authorities and both internal and external business partners regarding development and registration strategies. He/she will also lead development and implementation of department processes and policies. Essential Functions of the Job: Accountable for regulatory deliverables and milestones including the development of regulatory strategic and tactical plans. Provides strategic and operational regulatory direction on assigned projects including, but not limited to general regulatory strategies, regulatory requirements for clinical studies and marketing approval, risk assessments, critical issue management and advice on health authority interactions. Uses extensive knowledge of US, CAN, and ICH regulatory requirements with the ability to apply knowledge both strategically and with business needs and goals in mind. Responsible for managing decision-making, and conflict resolution surrounding regulatory issues within the Project Team. Responsible for ensuring appropriate escalation to functional management when necessary. Manage/oversee the preparation and submission of documentation to support investigational and marketing registration packages ensuring timelines are met. Review sections of IND/CTA, NDA/MAA, and other global submission documents in support of clinical trials and marketing applications, and their amendments in conformance with regulatory requirements and strategies. Liaise and negotiate with 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 regulatory environment and assess impact of changes on business and product development programs. Facilitate policy and development of standard interpretation of regulations. Integrates functional expertise with business knowledge to solve problems and make good decisions for the overall business. Qualifications: Bachelor’s degree with 8+ years’ of related regulatory experience is required. Preferred candidates will have experience working as a Project Lead in Regulatory Affairs, leading multiple FDA interactions. Experience should clearly be demonstrative of managerial, leadership, and collaboration ability across several functional areas. Ad vanced degree preferred. Experience with INDs/CTAs, NDAs/BLAs/MAAs, lifecycle management, interactions with Health Authorities, leading and managing regulatory teams, and developing and implementing regulatory strategies with a proven track record of accomplishments. Current knowledge of FDA perspectives, precedents, and guidances to drive shrewd and innovative regulatory strategies to support drug development. Thorough understanding of the drug development process, the pharmaceutical industry and healthcare environment including regulatory requirements and policy trends. Strong business acumen and ability to integrate multiple sources of data to make sound decisions that contribute positively to the business. Excellent verbal and written skills; able to analyze, define, and effectively convey difficult and complex issues in a way that accurately and persuasively communicates the issues to internal and external stakeholders. Skilled in conflict resolution/negotiation. Fosters open communication. Listens and facilitates discussion. Strong negotiating skills and ability to think creatively and develop creative solutions. Proven ability to build trust and respect within organization. Ability to prioritize and handle multiple projects simultaneously. Supervisory Responsibilities: Will line manage, and/or mentor, junior supporting staff. Train and develop an effective regulatory team both via direct and indirect reporting structure. Computer Skills: PC literacy required; proficient use of technology including MS Office skills (Outlook, Word, Excel, PowerPoint), document management systems, and Internet resources. Travel: N/A 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 Salary Range: $146,700.00 - $196,700.00 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. The Company has a comprehensive benefits package that includes Medical, Dental, Vision, 401(k), FSA/HSA, Life Insurance, Paid Time Off, and 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 [email protected] .