Global Applied Statistics & Analytics Head

Posted 18 Hours Ago
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Hiring Remotely in United States
Remote
Senior level
Biotech
The Role
The Global Applied Statistics & Analytics Head will lead the technical aspects of statistical analysis within Legend Biotech's MSAT organization. Responsibilities include establishing a Statistical Center of Excellence, providing mentorship, developing statistical analyses and models, ensuring compliance with cGMP processes, and collaborating globally to address complex technical problems in cell therapy manufacturing.
Summary Generated by Built In

Company Information

Legend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, New Jersey, we are developing advanced cell therapies across a diverse array of technology platforms, including autologous and allogenic chimeric antigen receptor T-cell and natural killer (NK) cell-based immunotherapy. 

Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of Johnson & Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel) in 2017. Our strategic partnership is designed to combine the strengths and expertise of both companies to advance the promise of an immunotherapy in the treatment of multiple myeloma.

Legend Biotech is seeking a Global Applied Statistics & Analytics Head as part of the Technical Operations team based Remote. 

Role Overview

This position is a lead technical role in the global MSAT organization. This individual will be responsible for all applied statistics and analytics scope in support of the approved Carvykti commercial process. This effort will extend to developing a center of excellence in cell therapy to drive global statistical approaches, methods and standards as well as the system and tools used in day to day commercial analyses. At a technical level, the candidate will be required to develop statistical analyses to solve complex, inter-dependent, multi-variate/factor technical problems and establish statistical models to correlate all process parameters. This effort is business critical to ensure that ongoing manufacturing processes are in a state of control and, additionally, adhere to guidelines established for CPV. In this role, it is expected to work closely with the site to gather data and reporting requirements and align tools/models/reporting mechanism globally for all manufacturing nodes. This effort would extend to development of end-to-end manufacturing data systems and include adopting leading GxP Part 11 tools from ingestion through reporting. Strong collaboration and partnership both internally and externally is required.

Key Responsibilities  

  • Build Statistical Center of Excellence intended to drive global statistical approaches and methods
  • Represent MSAT at joint statistical and analytical committee forums
  • Partner closely with global manufacturing sites to solve complex, inter-dependent, multi-variate/factor technical problems and establish statistical models to correlate all process parameters
  • Provide statistical and analytics mentorship/leadership for an expanding global manufacturing network for best-in-class CAR-T product
  • Provides applicable cell biology or cell therapy related statistics expertise as dedicated support to cell therapy SMEs and the vector programs
  • Develop statistical analyses
  • Provides advanced statistical analyses and development of simulation models (ie. predictive of risks to study failure)
  • Expertise and development of industry leading advanced statistical methods/tools, Machine Learning and AI tools
  • Serves as primary SME for Health Authority interactions, responses to agency questions (RFIs), drafting industry guidelines, support for revisions to specification & critical limits, and training
  • Works closely with the site to gather data and reporting requirements and aligns tools/models/reporting
  • Develops plans to build out end-to-end manufacturing data systems. Scope includes industry leading GxP Part 11 compliant analytical tools and systems from ingestion through reporting
  • Establishes global tiered data governance business processes to align across manufacturing nodes
  • Employs industry leading methodologies and standard approaches specific to cell therapy products (ie. modified Nelson/Shewart rules, Equivalence vs. Expectation approaches for comparability)
  • Drives justification and alignment with key partners (ie. JnJ)
Requirements
  • B.S. required, Ph.D. preferred in technical discipline: engineering, science, or related field
  • Minimum 12 years of industrial biologics CMC development or manufacturing experience, CAR-T experience is highly desirable.
  • Extensive experience in cell therapy commercial cGMP program with end-to-end know-how to manage process platform changes/improvements in a global manufacturing network and change management process.
  • Candidate must have extensive experience in Cell Therapy tech transfer and/or MSAT.
  • Extensive experience in a cross functional CMC team as a technical statistics and analytics representative supporting global commercial programs in cell therapy
  • Extensive experience employing statistical and analytical methods to solve complex manufacturing issues in cGMP
  • Experience in driving consistent statistical approaches and defending them to health authorities
  • Experience in collaborating with internal technical SMEs to develop pragmatic solutions and deliverables around validation and comparability
  • Industry leading knowledge in technology transfer, process comparability, CMC regulatory guidelines and manufacturing in cell therapy.
  • Ability to think critically and demonstrated troubleshooting and problem-solving skills.
  • Results driven with strong analytical, problem solving and critical thinking skills.
  • Strong experience working in a cross-functional organization with multiple partners with competing priorities.
  • Ability to plan, multitask, prioritize and be an effective and influential decision maker focused on action and implementation.
  • Language: English

#Li-Remote

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Legend Biotech is a proud equal opportunity/affirmative action employer committed to attracting, retaining, and maximizing the performance of a diverse and inclusive workforce. It is Legend’s policy to ensure equal employment opportunity without discrimination or harassment based on race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity or expression, age, disability, national origin, marital or domestic/civil partnership status, genetic information, citizenship status, uniformed service member or veteran status, or any other characteristic protected by law.

Legend Biotech maintains a drug-free workplace.

Top Skills

Machine Learning
Statistics
The Company
HQ: Somerset, New Jersey
1,192 Employees
On-site Workplace
Year Founded: 2014

What We Do

Legend Biotech is a global, commercial-stage biotechnology company developing and manufacturing novel therapies. We explore and apply innovative technologies to deliver cutting-edge options for patients around the world.

Our corporate headquarters is located in Somerset, NJ, and our manufacturing footprint includes facilities in the United States, China and the Belgium.

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