Senior Scientist/Principal Scientist, Quantitative Pharmacology (Contractor)
Company: Legend Biotech
Location: Somerset
Posted on: February 25, 2026
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Job 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 Senior
Scientist/Principal Scientist, Quantitative Pharmacology
(Contractor) as part of the Research & Early Development team based
in Somerset, NJ. Role Overview The position seeks a highly
motivated and experienced quantitative pharmacologist to lead
modeling and simulation efforts in support of gene and cell therapy
products, with a focus on QSP and popPK modeling (Prior cell and
gene therapy experience preferred). Contract Duration: 12 Months
Key Responsibilities Lead QSP and popPK modeling activities across
preclinical and clinical development stages. Play a pivotal role in
shaping clinical pharmacology strategies, supporting regulatory
submissions, and driving innovation in model-informed drug
development (MIDD). Develop and apply mechanistic models to
understand disease pathways, drug mechanisms, and patient
variability. Conduct simulations to support dose selection, trial
design, and exposure-response analyses. Collaborate
cross-functionally with R&D, clinical, regulatory, and
biostatistics teams. Author and review clinical pharmacology
sections of regulatory documents (e.g., INDs, NDAs). Contribute to
scientific publications and conference presentations. Requirements
R&D, Preclinical development, Clinical, CMC and regulatory
MS/PhD/Pharm D in Pharmaceutical Sciences, Clinical Pharmacology,
Applied Mathematics, Biomedical Engineering, or related
quantitative discipline. 7 years with MS degree or 3 years with
PhD/Pharm D degree of working experience in quantitative
pharmacology or pharmacometrics in pharmaceutical companies or CRO
companies (Job titles will be decided per applicant’s working
experience) Have strong execution ability Strong independent
scientific research ability, logical thinking, and
coordination/problem-solving skills Have clear written and oral
communication skills Have a good team spirit Demonstrated expertise
in QSP and popPK modeling, including proficiency with tools such as
NONMEM, R, MATLAB, Monolix, etc. Deep understanding of PK/PD
principles, translational medicine, and the role of quantitative
pharmacology and model-informed drug development (MIDD) in clinical
trials and drug development. Demonstrated ability and experience in
applying modelling and simulation approaches to enable rational and
efficient preclinical and clinical drug development. Familiar with
regulatory requirements and guidelines of clinical pharmacology.
Good project management skills, and the ability to collaborate with
other departments and manage with internal and external partners.
Proven track record of scientific contributions through
publications or presentations. Good personality, honest and
trustworthy. Physically and mentally healthy, love life. Li-JR1
Li-Contractor Li-Hybrid Please note: These benefits are offered
exclusively to permanent full-time employees. Contract employees
are not eligible for benefits through Legend Biotech. 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 policy, please review: Legend Biotech Privacy
Policy.
Keywords: Legend Biotech, New Brunswick , Senior Scientist/Principal Scientist, Quantitative Pharmacology (Contractor), Science, Research & Development , Somerset, New Jersey