Director of In Vivo Pharmacology at Legend Biotech

Philadelphia, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

13 Jan, 26

Salary

0.0

Posted On

15 Oct, 25

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

In Vivo Pharmacology, Cell Therapy, Gene Therapy, Cancer Models, Immunotherapy, Tumor Immunology, Cytokine Biology, T Cell Kinetics, Project Management, Cross-Functional Leadership, Data Presentation, Regulatory Documentation, Team Management, Emerging Technologies, Study Design, Mouse Handling

Industry

Biotechnology Research

Description

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. Legend Biotech is seeking Director of In Vivo Pharmacology as part of the Research & Early Development team based in Philadelphia, PA. Role Overview We are seeking an experienced and highly motivated Director of In Vivo Pharmacology to lead and expand our in vivo research capabilities in support of our cell and gene therapy pipeline. The successful candidate will be responsible for designing and overseeing preclinical pharmacology studies to evaluate the efficacy, safety, and mechanism of action of engineered cell or gene therapies in relevant in vivo models. This leadership role will be instrumental in guiding the transition of novel CAR-T candidates from discovery through IND-enabling studies and into early clinical development. Key Responsibilities Lead the strategic direction and execution of in vivo pharmacology studies supporting cell or gene therapy development programs. Design, develop, and validate in vivo models (e.g., xenograft, syngeneic, orthotopic) to evaluate CAR-T efficacy, persistence, trafficking, and toxicity. Oversee in vivo study execution in-house and at CROs, ensuring scientific rigor, quality, and compliance with regulatory standards. Work cross-functionally with discovery, translational biology, immunology, and clinical teams to integrate pharmacodynamic, biomarker, and mechanism-of-action data. Interpret and present data to internal stakeholders, executive leadership, and external collaborators or partners. Author key sections of regulatory documents (e.g., INDs, Investigator’s Brochures, study reports). Manage and mentor a team of scientists and research associates. Evaluate and implement emerging in vivo technologies and platforms to improve study throughput and translational relevance. The candidate has authority and should have the ability to make decisions on preclinical in vivo pharmacology strategies Requirements PhD, DVM in Pharmacology, Immunology, or related field, with 8+ years of relevant industry experience. Deep expertise in in vivo models of cancer and/or immunotherapy; experience with CAR-T, TCR, or other cell or gene therapies highly preferred. Strong understanding of tumor immunology, immune cell trafficking, cytokine biology, and T cell kinetics. Proven track record of leading IND-enabling pharmacology studies. Hands-on experience with mouse handling, tumor implantation, IV/SC dosing, and tissue processing is preferred. Demonstrated ability to lead cross-functional teams and external CRO collaborations. Excellent written and oral communication skills, with the ability to present complex data to both technical and non-technical audiences. Strong leadership, mentoring, and project management skills. #Li-JK1 #Li-Hybrid Benefits: We are committed to creating a workplace where employees can thrive - both professionally and personally. To attract and retain top talent in a highly competitive industry, we offer a best-in-class benefits package that supports well-being, financial stability, and long-term career growth. Our offerings are designed to meet the diverse needs of our team members and their families, ensuring they feel valued and supported every step of the way. Highlights include medical, dental, and vision insurance as well as a 401(k)-retirement plan with company match that vest fully on day one. Equity and stock options are available to employees in eligible roles, we offer eight weeks of paid parental leave after just three months of employment, and a paid time off policy that includes 15 vacation days, 5 personal days, 5 sick days, 11 U.S. national holidays, and 3 floating holidays. Additional 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 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. EEO Statement 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 applicable law. Employment is at-will and may be terminated at any time with or without cause or notice by the employee or the company. Legend may adjust base salary or other discretionary compensation at any time based on individual, team, performance, or market conditions. Legend Biotech maintains a drug-free workplace.

Responsibilities

The Director of In Vivo Pharmacology will lead and expand in vivo research capabilities to support cell and gene therapy pipeline. This role involves designing and overseeing preclinical pharmacology studies to evaluate the efficacy, safety, and mechanism of action of engineered therapies.