BeiGene, Ltd.

Associate Director / Director Global Clinical Process Management Lead

BeiGene, Ltd.$143K — $193K *
US-AnywhereRemote in United States
Pharmaceuticals & Biotech
8 - 10 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree required, ideally in science/healthcare; advanced degree preferred.
  • 8+ years of experience in the pharmaceutical or biotech sectors.
  • Extensive knowledge of clinical operations processes and ICH-GCP compliance management.
  • Experience in clinical trial process design, harmonization, and optimization.
  • Proven success in a matrix environment and collaboration within global teams.
  • Strong interpersonal, problem-solving, negotiation, and conflict resolution skills.
  • Effective written and oral communication skills, including strong presentation abilities.

Responsibilities

  • Execute global clinical process management activities to enhance efficiency and compliance.
  • Serve as the main contact for specific GCO processes related to standard operating procedures.
  • Develop content in collaboration with global process owners and technical writers for procedural documents.
  • Lead GCO process management projects, focused on continuous improvement and change management.
  • Promote and implement innovative ideas that enhance GCO processes and collaboration.
  • Oversee document review and approval workflows.
  • Advise on and review interdepartmental processes that affect GCO standards.
  • Contribute to training material development for GCO processes.

Benefits

  • Comprehensive medical, dental, and vision coverage.
  • 401(k) plan with company contributions.
  • Flexible spending accounts (FSA/HSA) available.
  • Life insurance and wellness programs.
  • Paid time off and employee stock purchase plan.
  • Eligibility for annual bonus and discretionary equity awards.
Full Job Description

General Description:

The Global Clinical Process Management Lead is responsible for leading and supporting global clinical process management activities within Global Clinical Operations. Working collaboratively with GCO stakeholders globally, this role promotes efficient, consistent, sustainable, and compliant processes and standards across GCO, while supporting innovative ideas that strengthen processes and ensuring effective alignment and follow-through from concept through implementation. The role also ensures alignment with ICH-GCP and applicable regulatory requirements.

Responsibilities:

  • Execute global clinical process management activities within GCO to promote efficiency, consistency, sustainability, and compliance with applicable regulatory requirements across GCO processes and standards.
  • Serve as the primary GCOE point of contact for one or more GCO processes, including SOPs, Work Instructions, and related standards.
  • Contribute to content development and collaborate with GCO Global Process Owners and Subject Matter Experts, or act as the Global Process Owner as appropriate, in the technical writing of GCO procedural documents, including SOPs, Work Instructions, templates, and tools.
  • Lead GCO process management initiatives in collaboration with GCPC, including assessing the need to revise or create controlled documents and supporting continuous improvement, change management, and implementation activities.
  • Identify, support, and help advance innovative ideas that improve GCO processes, enabling effective evaluation, stakeholder alignment, and follow-through from concept through implementation.
  • Lead document review and approval workflows.
  • Advise on and review processes owned by other functions that impact GCO processes and related standards.
  • Establish and maintain effective partnerships with relevant GCO and cross-functional groups, including GCP Compliance, Learning and Development, and other stakeholders as needed.
  • Contribute to the development and strategic direction of training materials related to GCO processes.

Supervisory Responsibilities:

  • Matrix supervisory

Computer Skills: 

  • Efficient in Microsoft suite (Excel, Outlook, Word, PowerPoint, Project)

Other Qualifications:

  • Fluent English (Oral; Written)
  • Relevant Bachelor’s degree minimum – preferred science/healthcare discipline
  • Minimum of 8 years of experience in pharmaceutical and/or biotechnology sector
  • Extensive knowledge of clinical operations process, ICH-GCP and compliance management; including application of clinical trial regulation/s
  • Experience in clinical trial process design, harmonization/optimization and implementation.
  • Experience working in matrix environment and in global teams
  • Excellent interpersonal, problem-solving, negotiation and conflict resolution skills
  • Excellent organizational skills and a pre-disposition to quality management and process improvement
  • Effective communicator (oral and written)
  • Strong presentation skills

Education Required:

  • Bachelor’s degree required, master’s degree or other relevant post graduate qualification 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

Salary Range: $143,300.00 - $193,300.00 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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