BeiGene, Ltd.

Senior Manager, Regulatory Affairs

BeiGene, Ltd.$139K — $184K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • 7+ years' experience in regulatory affairs with a BA/BS degree.
  • Expertise in preparing INDs and familiarity with NDAs, amendments, and supplements.
  • Proficient in CTD/eCTD formats and Adobe Acrobat Professional.
  • Strong knowledge of FDA and ICH regulations, with understanding of FDA structure.
  • Working knowledge of GMP, GLP, and GCP regulations relevant to the pharmaceutical lifecycle.
  • Excellent communication and planning skills, detail-oriented and self-motivated.

Responsibilities

  • Plan and manage regulatory activities for complex projects with minimal supervision.
  • Develop strategies for expedited approvals of regulatory submissions.
  • Oversee writing, assembling, reviewing, and submitting regulatory dossiers domestically and internationally.
  • Ensure compliance of regulatory submissions and manage the preparation of meeting requests.
  • Supervise the compilation and submission of INDs, BLAs/NDAs, and safety reports, providing regulatory expertise to project teams.
  • Maintain up-to-date regulatory knowledge and compliance within the department.

Benefits

  • Medical, Dental, and Vision coverage.
  • 401(k) plan with company contributions.
  • Flexible Spending Account (FSA) and Health Savings Account (HSA) options.
  • Life Insurance and Paid Time Off (PTO).
  • Wellness programs and employee stock purchase options.
Full Job Description
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 timely planning and coordination of regulatory submissions and provide guidance to cross-functional teams on regulatory strategy and tactics. The Manager will represent Regulatory Affairs on cross-functional project teams, will provide input to the project team, will lead authoring and preparation of annual reporting, and will manage regulatory submissions.

Essential Functions of the Job:
  • With minimal supervision, plan and manage regulatory activities related to assigned projects that span technical areas including clinical, non-clinical, and CMC
  • Assist in developing and implementing strategies for the earliest possible approvals/clearance of regulatory submissions associated with assigned projects
  • Manage the preparation, including writing as necessary, assembly, review, and timely submission of regulatory dossiers as required for investigation and registration of products in the US and abroad
  • Ensure regulatory submissions are maintained in compliance with regulatory requirements. Support and manage preparation of meeting requests and briefing documents
  • Manage the preparation, review, and submission of all components of regulatory submissions including INDs and amendments, BLAs/NDAs and supplements, annual reports, safety reports, etc. Participate on project teams and provide expertise on regulatory matters
  • Develop and maintain current regulatory knowledge and advise management of significant developments. Ensure compliance with departmental requirements including and maintenance of regulatory archive. Work with external regulatory consultants/CRO's as required

Qualifications:
  • 7+ years' related experience with a BA/BS degree is required
  • Experience and knowledge in preparation of INDs (required) and NDAs (desirable), and supportive amendments and supplements (manufacturing, nonclinical, clinical)
  • Experience with CTD/eCTD
  • Experience with publishing documents in Adobe Acrobat Professional
  • Working knowledge of FDA and ICH regulatory guidance and regulations.
  • Understanding of FDA structure and function
  • Knowledge/experience with regulatory requirements for other regions also desirable
  • Working knowledge of GMP, GLP, and GCP regulations as well an understanding of the pharmaceutical product life cycle.
  • Excellent oral and written communications skills are a must as are superior planning skills
  • The candidate should be detail-oriented, a self-starter, and be comfortable with broad responsibilities in an entrepreneurial, fast-paced, small company environment


Supervisory Responsibilities:

NA

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: $139,800.00 - $184,800.00 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.

About BeiGene, Ltd.

BeiGene, Ltd. is a biotechnology company that develops and commercializes innovative cancer treatments. The company was founded in 2010 and is headquartered in George Town, Grand Cayman. BeiGene's portfolio includes several drug candidates that target cancer cells and the tumor microenvironment. The company's lead product, Brukinsa, is a treatment for mantle cell lymphoma that has been approved by the U.S. Food and Drug Administration (FDA) and the European Medicines Agency (EMA). BeiGene also has partnerships with several pharmaceutical companies, including Amgen, Merck, and Novartis.
Learn more about BeiGene, Ltd.
Size
8,300 employees
Market Cap
$22.2 billion
Industry
Net Income
-$1.5 billion
Founded
2010
5 Year Trend
+305.7%
Revenue
$308.8 million
NASDAQ

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