Sr. Clinical Research Scientist
Confirmed live in the last 24 hours
Legend Biotech

1,001-5,000 employees

Develops and manufactures novel cell therapies globally
Company Overview
Legend Biotech, a global biotechnology company, stands out due to its comprehensive approach to cell therapy, extending from discovery to commercialization, and its commitment to treating intractable and incurable diseases. The company's leadership boasts significant expertise from major pharmaceutical companies, and it offers a variety of career opportunities that contribute to the development of novel therapies. With facilities in the United States, China, and Belgium, Legend Biotech is dedicated to utilizing four different technologies to target hematologic malignancies and solid tumors, demonstrating its adaptability and commitment to personalized medicine.

Company Stage


Total Funding





Franklin Township, New Jersey

Growth & Insights

6 month growth


1 year growth


2 year growth

Somerset County, NJ, USA
Experience Level
Desired Skills
Biology & Biotech
  • Bachelor’s degree is required in life science discipline.
  • Bachelor’s degree with 4+ years’; or MS with 3+ years’; or PharmD/PhD with 2+ years of pharma experience in clinical development or related function.
  • Good interpersonal & communication skills, including oral, written and interpersonal.
  • Ability to effectively manage conflicts and negotiations while providing impact and influence
  • Collaborative with the ability to operate across multiple geographies
  • Good leadership & organizational skills, analytical skills, and presentation skills
  • Creative problem-solving skills
  • Strong organizational and project management skill and the ability to multitask
  • Computer literacy required (MS word, MS excel, MS PowerPoint and MS Project)
  • Oncology Therapeutic Experience preferred
  • Responsible to ensure the data review and cleaning activities meet the quality standards to support database locks in collaboration with data management and medical lead/clinical trial lead. Uses clinical and disease state knowledge to make recommendations for methods and strategy for data cleaning approach
  • Collaborate with other functions to successfully support the planning and execution of clinical studies. Provides independent leadership of all areas requiring clinical input with oversight from the assigned Clinical Trial Lead/Medical Lead, and provides innovative and quality solutions for assigned problems and tasks.
  • Provides clinical input and strategic recommendations for the planning and implementation of assigned clinical trial(s) including investigator selection, patient recruitment, feasibility questionnaire, training PowerPoints, and supporting Ethics committee submissions.
  • Contributes to the strategic planning, preparation, and review of clinical documents (Protocol, ICFs, CSR, investigator brochure). May lead certain documents or sections of documents, including incorporation of input from other cross-functional team members.
  • Provides clinical input and strategic recommendations for regulatory documents needed for all stages of assigned trial lifecycle (IND documentation, HA briefing books, BLAs, and Orphan Drug Applications)
  • Responsible for clinical portions of key data management/statistical documents (eg: Case Report Forms, edit checks, data review plan and reports)
  • Contribute to the planning and execution of external meetings and internal stakeholder meetings (e.g., Ad Boards, IMs, Governance, DMCs, Regulatory Authority, Dose Escalation meeting); responds to or triages questions for appropriate escalations. May have a speaking role on meetings when appropriate.
  • Supports their manager when asked to contribute to harmonization between clinical trials and process improvement initiatives.
Desired Qualifications
  • Oncology Therapeutic Experience