Jobs Companies Legend Biotech US Sr. Director, Medical Excellence & Operations

Über diese Sr. Director, Medical Excellence & Operations Stelle bei Legend Biotech US

Legend Biotech US · Vor Ort · Somerset, New Jersey, United States

Legend Biotech is a global biotechnology company dedicated to treating and, one day, curing life-threatening diseases. Headquartered in Bridgewater, New Jersey, we are advancing the next generation of cell therapy through a portfolio of innovative technologies, including autologous, allogeneic, and in vivo cell therapy approaches. Our research spans chimeric antigen receptor T-cell (CAR-T), T-cell receptor (TCR-T), natural killer (NK) cell-based therapies, and other emerging platforms designed to transform the treatment of serious diseases. From our global network of research and development sites, we are committed to discovering and developing safe, effective, and cutting-edge therapies for patients worldwide.

Legend Biotech entered into a global collaboration agreement with Johnson & Johnson to jointly develop and commercialize CARVYKTI® (ciltacabtagene autoleucel; cilta-cel). Through this strategic partnership, we combine complementary expertise and capabilities to advance innovative immunotherapies for patients living with multiple myeloma.

Legend Biotech is seeking a Sr. Director, Medical Excellence & Operations as part of the Medical Affairs team based Remotely. 

Role Overview

The Sr. Director, Medical Excellence & Operations is responsible for developing and driving the vision, strategy, and executional excellence of Medical Affairs operations across the organization. This role ensures Medical Affairs functions as a high-performing, compliant, and strategically aligned enterprise capability, enabling scientific leadership and impactful stakeholder engagement across product lifecycles.

Operating as a key member of the Medical Affairs Leadership Team (MALT), this leader owns the end-to-end Medical Excellence operating model, including governance, resourcing, execution of Medical initiatives internally and externally (e.g., congresses, medical exhibits, education, sponsorships, engagements), operational platforms, and continuous capability advancement. The role partners closely with Clinical Development, Commercial, Legal, Compliance, Finance, Procurement, and external collaborators to translate medical strategy into flawless execution at scale.

Key Responsibilities

  • Define and own the Medical Excellence & Operations strategy, ensuring alignment with Medical Affairs vision, portfolio priorities, and long-term business objectives.
  • Serve as a strategic advisor to the VP of Medical Affairs and Medical Affairs Leadership Team, providing operational insights, risk mitigation strategies, and executional foresight.
  • Collaborate with partner company (alliance JNJ) to advance current indications and future launch strategies by aligning shared Medical Affairs priorities, coordinating cross-functional planning, and ensuring operational readiness for key milestones across the product lifecycle. 
  • Partner with Digital Lead to operationalize transformative initiatives to mature capabilities, scalability, and readiness for growth, launches, and evolving scientific needs.
  • Establish and maintain robust governance frameworks for Medical Affairs activities, ensuring consistent compliance with Legal, Regulatory, and corporate policies across all medical activities.
  • Ensure organizational readiness for audits and inspections through standardized processes, documentation rigor, and continuous oversight.
  • Function as a senior escalation point for complex operational, compliance, or budgetary decisions impacting Medical Affairs.
  • Provide executive oversight for medical congress strategy and execution, medical education, and sponsorship programs.
  • Ensure Medical initiatives are delivered with scientific integrity, operational excellence, and budget discipline, while meeting timelines and strategic objectives.
  • Partner with the MALT to enable seamless execution of activities and measurement of impact.
  • Own key components of the Medical Affairs operating budget, ensuring transparency, efficiency, and value optimization.
  • Oversee vendor strategy, contracting models, and resource allocation to support Medical Affairs execution at scale.
  • Collaborate with Finance and Procurement to forecast resource needs, manage spend, and continuously optimize cost structures.
  • Provide executive sponsorship and accountability for Medical Affairs operational platforms (e.g., grants & sponsorship portals, nomination portal.
  • Contribute to KPIs, dashboards, and performance metrics to measure executional effectiveness, cycle times, quality, and organizational impact. 
  • Drive a culture of data-informed decision-making and continuous improvement.
  • Build, lead, and develop a high-performing Medical Excellence & Operations organization, including the Senior Project Manager, Medical Affairs Managers, Sr Coordinator and Medical Affairs Intern.
  • Establish clear expectations, career paths, and development plans to grow internal talent and succession pipelines.
  • Foster a culture of accountability, collaboration, and continuous improvement across Medical Affairs operations.

Requirements

  • A bachelor's degree is required and possessing an advanced degree or completed leadership training is desired.
  • 10+ years of experience in Medical Affairs, Medical Operations, or pharmaceutical/biotech leadership roles, with demonstrated success leading complex, enterprise-level initiatives.
  • Proven track record of building and scaling Medical Affairs operational capabilities in a highly regulated environment.
  • Senior level leadership and influence across matrixed organizations.
  • Deep understanding of Medical Affairs governance, compliance, and scientific engagement models.
  • Strong financial acumen with experience managing budgets, vendors, and operating plans.
  • Excellent strategic thinking, change leadership, and decision-making capabilities.
  • Exceptional communication skills with the ability to engage and collaborate with senior stakeholders.

#Li-JK1

#Li-Remote

The base pay range below is what Legend Biotech USA Inc. reasonably expects to offer at the time of posting. Actual compensation may vary based on experience, skills, qualifications, and geographic location. The company reserves the right to modify this range as needed and in accordance with applicable laws.

Other Types of Pay: Performance-based bonus and/or equity is available to employees in eligible roles.

Benefits and Paid Time Off: Medical, dental, and vision insurance as well as a 401(k) retirement plan with a company match that vests fully on day one. We offer eight (8) weeks of paid parental leave after just three (3) months of employment, and a paid time off policy that includes vacation time, personal time, sick time, floating holidays, and eleven (11) company holidays. Additional voluntary benefits include flexible spending and health savings accounts, life and AD&D insurance, short- and long-term disability coverage, legal assistance, and supplemental plans such as pet, critical illness, accident, and hospital indemnity insurance. We also provide voluntary commuter benefits, family planning and care resources, well-being initiatives, and peer-to-peer recognition programs; demonstrating our ongoing commitment to building a culture where our people feel empowered, supported, and inspired to do their best work.

Pay Range (Base Pay):
$222,672$292,258 USD

Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.

Work Authorization & Employment Eligibility

Applicants must be authorized to work in the United States. As part of our commitment to maintaining a lawful workforce and ensuring compliance with federal employment regulations, we participate in the E-Verify program. If you are selected for employment, you will be required to complete the Form I-9 process, and your employment eligibility will be verified through E-Verify in accordance with applicable federal law. We are committed to providing a fair, transparent, and welcoming hiring experience for all candidates.

EEO Statement

It is the policy of Legend Biotech to provide equal employment opportunities without regard to actual or perceived race, color, creed, religion, national origin, ancestry, citizenship status, age, sex or gender (including pregnancy, childbirth, related medical conditions and lactation), gender identity or gender expression (including transgender status), sexual orientation, marital status, military service and veteran status, disability, genetic information, or any other protected characteristic under applicable federal, state or local laws or ordinances.

Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company.

For information related to our privacy notice, please review: Legend Biotech Privacy Notice.
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Über Legend Biotech US

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, T-cell receptor (TCR-T), and natural killer (NK) cell-based immunotherapy. From our three R&D sites around the world, we apply these innovative technologies to pursue the discovery of safe, efficacious and cutting-edge therapeutics for patients worldwide.  

 

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). 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.

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