Legend Biotech Corporation

Sr. Scientist, Toxicology

Legend Biotech Corporation$127K — $167K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Ph.D., DVM, PharmD, or equivalent degree in Toxicology, Pharmacology, Immunology, or related discipline.
  • Minimum of 5 years' experience in nonclinical toxicology within biotech or pharmaceutical R&D.
  • Experience with cell therapy, gene therapy, or biologics is preferred.
  • Familiarity with GLP studies, CRO management, and regulatory expectations for nonclinical development.
  • Knowledge of FDA, EMA, and ICH regulations related to toxicology and advanced therapies.

Responsibilities

  • Support nonclinical toxicology activities for cell and gene therapy programs.
  • Design, monitor, and report on pharmacology and toxicology studies.
  • Contribute to data interpretation for candidate selection and risk assessment.
  • Execute study strategies at CROs, including protocol and report reviews.
  • Collaborate with cross-functional teams to further development programs.
  • Prepare regulatory documents for submissions and health authority responses.
  • Interpret complex datasets and communicate findings to stakeholders.

Benefits

  • Medical, dental, and vision insurance.
  • 401(k) retirement plan with a full company match on day one.
  • Eight weeks of paid parental leave after just three months of employment.
  • Paid time off including vacation, personal, sick days, and holidays.
  • Voluntary benefits such as health savings accounts and life insurance.
Full Job Description
Sr. Scientist, Toxicology Legend Biotech is seeking a Sr. Scientist, Toxicology as part of the Early Drug Development team based in Somerset, NJ or Philadelphia, PA. Role Overview Legend Biotech is seeking a Sr. Scientist, Toxicology to support nonclinical development and safety assessment across cell and gene therapy programs. This individual will contribute to nonclinical strategy from discovery through IND-enabling development and support regulatory submissions for innovative advanced therapies. The role requires scientific expertise in toxicology, a foundation in pharmacology, understanding of regulatory expectations, and the ability to work effectively across cross-functional teams in a fast-paced biotech environment. Key Responsibilities • Support toxicology activities for discovery and development-stage cell and gene therapy programs. • Design, monitor, interpret, and report nonclinical safety, pharmacology, biodistribution, and pharmacokinetic studies. • Support integrated interpretation of toxicology and pharmacology data to enable candidate selection, risk assessment, and program progression. • Contribute to study strategy and execution at CROs, including protocol review, study monitoring, data interpretation, and final report review. • Partner closely with Pharmacology, CMC, Clinical, Regulatory Affairs, and Program Management teams to advance development programs. • Support preparation of regulatory documents, including briefing packages, pre-IND/IND submissions, investigator brochures, and responses to health authority questions. • Contribute to safety risk assessments related to target biology, exaggerated pharmacology, off-target effects, immunogenicity, genome-related risks, and long-term safety. • Interpret complex nonclinical datasets and communicate key findings and recommendations clearly to internal stakeholders. • Stay current with scientific and regulatory advances relevant to toxicology, pharmacology, and cell and gene therapy development. • Support in vivo pharmacology activities, when needed, through integrated assessment of efficacy, disposition, and safety findings. Requirements • Ph.D., DVM, PharmD, or equivalent degree in Toxicology, Pharmacology, Immunology, or a related discipline. • Minimum of 5 years of experience in nonclinical toxicology or a related field within biotechnology or pharmaceutical R&D, with working knowledge of pharmacology principles. • Experience supporting cell therapy, gene therapy, biologics, or other advanced therapeutic platforms preferred. • Working knowledge of GLP toxicology studies, nonclinical pharmacology studies, CRO management, and regulatory expectations for nonclinical development. • Experience contributing to IND/CTA-enabling packages and global regulatory submissions is highly desirable. • Understanding of FDA, EMA, and ICH regulations pertaining to toxicology and cell and gene therapy development. • Scientific writing, communication, and presentation skills. • Ability to work independently while thriving in a collaborative, matrixed team environment. #Li-JR1 #Li-Hybrid 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): $127,313-$167,099 USD Please note: These benefits are offered exclusively to permanent full-time employees. Contractors are not eligible for benefits through Legend Biotech.

About Legend Biotech Corporation

Legend Biotech Corporation is a clinical-stage biopharmaceutical company focused on developing innovative cell therapies for cancer. The company's lead product candidate, LCAR-B38M/JNJ-68284528, is a chimeric antigen receptor (CAR) T-cell therapy that is being developed for the treatment of multiple myeloma, a type of blood cancer. Legend Biotech was founded in 2014 as a subsidiary of GenScript Biotech Corporation and became an independent company in 2019. The company is headquartered in Shanghai, China and has operations in the United States and Europe.
Learn more about Legend Biotech Corporation
Size
1,071 employees
Market Cap
$8.2 billion
Industry
NASDAQ

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