What are the responsibilities and job description for the Sr. Principal Scientist/Associate Director of Clinical Pharmacology position at Legend Biotech US?
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 Sr. Principal Scientist / Associate Director of Clinical Pharmacology as part of the Research and Early Development team based in Somerset, NJ.
Role Overview
The position functions as the leader of clinical pharmacology to support cell therapy drug development (prior experience with gene and cell therapy products preferred).
Key Responsibilities
- Function as clinical pharmacology representative in the project team and support clinical pharmacology-related activities in clinical studies, including protocol design, study implementation, data analysis, reports writing and regulatory submissions, etc.
- Ensure that clinical pharmacology strategy is developed, aligned with cross-function team, endorsed and executed to support the pipeline development
- Coordinate and monitor clinical pharmacology data to ensure all execution is in line with departmental strategy, in compliance with regulatory and legal requirements, and company standard operating procedures.
- Conduct pharmacokinetic (PK) / pharmacodynamic (PD) and dose-exposure-response analysis to support dose selection, trial design, internal decision-making, regulatory submissions, and published articles.
- Provide advice for preclinical stage projects to optimize in vitro and preclinical data, support projects to advance clinical development and submit new drug applications.
- Writing clinical pharmacology-related documents, oral communication, and presentation, etc.
- Key Relationships : R&D, Preclinical development, Clinical, CMC and regulatory
Requirements
Have strong execution ability;
Deep understanding of PK, PD, PK / PD, and / or Translational Medicine and the role of clinical pharmacology in clinical trials and drug development.
Good personality, honest and trustworthy;
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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.
